Faster access than browser!
303 relations: Absinthin, Acetylenedicarboxylic acid, Acrolein, Acrylonitrile, Alder (surname), Aldrin, Alkene, Alkyne, Alkyne trimerisation, Anthracene, Anthraquinone, Antiaromaticity, Aromatic hydrocarbon, Aromatization, Arsabenzene, Aryne, Ascaridole, Atom economy, Aza-Diels–Alder reaction, Azomethine ylide, Barrelene, Basketene, Bentley compounds, Benzocyclobutadiene, Benzofuran, Benzylamine, Benzylideneacetone, Betaenone B, Biomimetic synthesis, Bioorthogonal chemistry, Bisoxazoline ligand, Borabenzene, Bradsher cycloaddition, BTBP, Buckminsterfullerene, Butyl group, Captodative effect, Carbon nanotube chemistry, Carbon–carbon bond, Carpanone, CBS catalyst, Chaetoglobosin A, Cheletropic reaction, Chemical reaction, Chiral auxiliary, Chiral Lewis acid, Chlordane, Chlorendic acid, Cholesterol total synthesis, Christopher Spencer Foote, ..., Chromium(III) chloride, Click chemistry, Coarctate reaction, Codinaeopsin, Copper(II) tetrafluoroborate, Copper(II) triflate, Cracking (chemistry), Criegee oxidation, Cubane, Cyclacene, Cyclic compound, Cycloaddition, Cycloalkane, Cycloalkyne, Cyclobutadiene, Cyclobutadieneiron tricarbonyl, Cycloheptatriene, Cyclohexene, Cyclohexenone, Cycloisomerization, Cyclopentadiene, Cyclopentenone, Cyclophane, Cyclopropene, Cytochalasin B, Danishefsky's diene, Dechlorane plus, Dendralene, Dendrimer, Deoxyribozyme, Deutzer Friedhof, Dicoronylene, Dicyanoacetylene, Dicyclopentadiene, Dieldrin, Diels, Diels–Alder reaction, Diene, Diethyl azodicarboxylate, Diethyl oxomalonate, Dimer (chemistry), Dimethyl acetylenedicarboxylate, Dimethyl carbate, Dimethylbutadiene, Diphosphorus, Discodermolide, DNA-encoded chemical library, Dodecahedrane, Dynamic combinatorial chemistry, Electrocyclic reaction, Electronic effect, Elias James Corey, Elisabeth Dane, Endiandric acid C, Endohedral fullerene, Endohedral hydrogen fullerene, Endosulfan, Ene reaction, Enol ether, Enone, Ethyl acrylate, Ethylidene norbornene, EuFOD, Fencamfamin, Foldit, Frontier molecular orbital theory, Fullerene chemistry, Fulvalene, Fumaric acid, Furan, Glutaraldehyde, Gold(III) bromide, Hagemann's ester, Heptacene, Heptachlor, Hexabenzocoronene, Hexachlorocyclopentadiene, Hexadehydro Diels-Alder reaction, Hexafluoro-2-butyne, Hexafluoroisobutylene, Hexaphenylbenzene, Himbacine, HOMO/LUMO, Hydrogen-bond catalysis, Imine Diels–Alder reaction, In-Methylcyclophane, Indenofluorene, Indium(III) chloride, Indole, Integrasone, Intramolecular Diels–Alder cycloaddition, Inverse electron-demand Diels–Alder reaction, Ionic liquid, Iridoid, Isocyanate, IUPAC nomenclature for organic transformations, Jacobsen's catalyst, Kurt Alder, Lactam, Lanthanide trifluoromethanesulfonates, Lawesson's reagent, Lewis acid catalysis, Limonene, Linseed oil, List of German inventions and discoveries, List of German inventors and discoverers, List of Nobel laureates in Chemistry, List of organic reactions, Lithium perchlorate, Lovastatin, M. Christina White, Macrophomic acid, Maleic acid, Maleic anhydride, Maleimide, Marshall D. Gates Jr., Mesembrine, Metal-centered cycloaddition reactions, Methyl acrylate, Methylcyclopentadiene, Methylene blue, Mevastatin, Michael E. Jung, Montréalone, Myrcene, Myrcenol, N-Sulfinylaniline, Name reaction, Naphthalene, Neighbouring group participation, Nicolaou Taxol total synthesis, Niobium(V) chloride, Nitroalkene, Nitrosobenzene, Norbadione A, Norbornadiene, Norbornene, Nosiheptide, On water reaction, Organic acid anhydride, Organic reaction, Organocatalysis, Organogold chemistry, Organoiron chemistry, Oripavine, Oseltamivir total synthesis, Otto Diels, Outline of organic chemistry, Oxanorbornadiene, Oxazole, Oxo-Diels–Alder reaction, Oxocarbenium, Phosphaalkene, Phosphole, Photochemistry, Photoredox catalysis, Physical organic chemistry, Podophyllotoxin, Polyacetylene, Potential applications of graphene, Prato reaction, PRIME (PRobe Incorporation Mediated by Enzymes), Prismane, Process chemistry, Protein design, Pyramidal alkene, Pyrene, Pyrrole, Pyrylium salt, Quaternary carbon, Retro-Diels–Alder reaction, Ring forming reaction, Robert Burns Woodward, Rubicordifolin, Rubottom oxidation, RXNO Ontology, Saegusa–Ito oxidation, Salvinorin A, Scientific phenomena named after people, Self-healing material, Shibasaki catalysts, Silabenzene, Silsesquioxane, Singlet oxygen, Stannabenzene, Stereoelectronic effect, Stereospecificity, Stille reaction, Strychnine total synthesis, Sulfene, Sulfolene, Sulfur diimide, Supramolecular catalysis, Tetrahydrobenzaldehyde, Tetrahydrophthalic anhydride, Tetramethyl acetyloctahydronaphthalenes, Tetraphenylcyclopentadienone, Tetrazine, Tetrodotoxin, Thermal scanning probe lithography, Thermodynamic versus kinetic reaction control, Thial, Thiazole, Thiobenzophenone, Thioketone, Thiophene, Thiophosgene, Tilidine, Timeline of biology and organic chemistry, Torreyanic acid, Total synthesis of morphine and related alkaloids, Triazine, Tricyclobutabenzene, Triflate, Trifluoroperacetic acid, Trimetasphere, Tripamide, Triptycene, Tropone, Ugi reaction, Umpolung, Vicinal difunctionalization, Vinyl acetate, Vinyl norbornene, Vinylcyclopropane rearrangement, Vinyldithiin, Vinylene carbonate, Vitamin B12 total synthesis, Wagner-Jauregg reaction, Water, William R. Roush, Woodward–Hoffmann rules, Ytterbium, Yuehchukene, Zirconium(IV) chloride, 1,2,3,4-Tetraphenylnaphthalene, 1,2,4,5-Tetrabromobenzene, 1,2-Cyclohexane dicarboxylic acid diisononyl ester, 1,3-Butadiene, 1,3-Cyclohexadiene, 1,3-Dipolar cycloaddition, 1,4-Benzoquinone, 1,4-Dioxin, 1,4-Naphthoquinone, 1,7-Octadiene, 1928 in science, 2,5-Dimethylfuran, 2-Pyrone, 3-Bromofuran, 4+3 cycloaddition, 4,7-Dihydroisoindole, 4-Phenyl-1,2,4-triazole-3,5-dione, 4-Vinylcyclohexene. Expand index (253 more) »
Absinthin
Absinthin is a naturally produced triterpene lactone from the plant Artemisia absinthium (Wormwood).
New!!: Diels–Alder reaction and Absinthin · See more »
Acetylenedicarboxylic acid
Acetylenedicarboxylic acid or butynedioic acid is an organic compound (a dicarboxylic acid) with the formula C4H2O4 or HO2C-C≡C-CO2H.
New!!: Diels–Alder reaction and Acetylenedicarboxylic acid · See more »
Acrolein
Acrolein (systematic name: propenal) is the simplest unsaturated aldehyde.
New!!: Diels–Alder reaction and Acrolein · See more »
Acrylonitrile
Acrylonitrile is an organic compound with the formula CH2CHCN.
New!!: Diels–Alder reaction and Acrylonitrile · See more »
Alder (surname)
Alder is a surname.
New!!: Diels–Alder reaction and Alder (surname) · See more »
Aldrin
Aldrin is an organochlorine insecticide that was widely used until the 1990s, when it was banned in most countries.
New!!: Diels–Alder reaction and Aldrin · See more »
Alkene
In organic chemistry, an alkene is an unsaturated hydrocarbon that contains at least one carbon–carbon double bond.
New!!: Diels–Alder reaction and Alkene · See more »
Alkyne
In organic chemistry, an alkyne is an unsaturated hydrocarbon containing at least one carbon—carbon triple bond.
New!!: Diels–Alder reaction and Alkyne · See more »
Alkyne trimerisation
An alkyne trimerisation reaction is a 2+2+2 cyclization reaction in which three molecules of alkyne react to form an arene.
New!!: Diels–Alder reaction and Alkyne trimerisation · See more »
Anthracene
Anthracene is a solid polycyclic aromatic hydrocarbon (PAH) of formula C14H10, consisting of three fused benzene rings.
New!!: Diels–Alder reaction and Anthracene · See more »
Anthraquinone
Anthraquinone, also called anthracenedione or dioxoanthracene, is an aromatic organic compound with formula.
New!!: Diels–Alder reaction and Anthraquinone · See more »
Antiaromaticity
Antiaromaticity is a characteristic of a cyclic molecule with a π electron system that has higher energy due to the presence of 4n electrons in it.
New!!: Diels–Alder reaction and Antiaromaticity · See more »
Aromatic hydrocarbon
An aromatic hydrocarbon or arene (or sometimes aryl hydrocarbon) is a hydrocarbon with sigma bonds and delocalized pi electrons between carbon atoms forming a circle.
New!!: Diels–Alder reaction and Aromatic hydrocarbon · See more »
Aromatization
Aromatization is a chemical reaction in which an aromatic system is formed.
New!!: Diels–Alder reaction and Aromatization · See more »
Arsabenzene
Arsabenzene (IUPAC name: arsinine) is an organoarsenic heterocyclic compound with the chemical formula C5H5As.
New!!: Diels–Alder reaction and Arsabenzene · See more »
Aryne
Arynes or benzynes are highly reactive species derived from an aromatic ring by removal of two ortho substituents.
New!!: Diels–Alder reaction and Aryne · See more »
Ascaridole
Ascaridole is a natural organic compound classified as a bicyclic monoterpene that has an unusual bridging peroxide functional group.
New!!: Diels–Alder reaction and Ascaridole · See more »
Atom economy
Atom economy (atom efficiency) is the conversion efficiency of a chemical process in terms of all atoms involved and the desired products produced.
New!!: Diels–Alder reaction and Atom economy · See more »
Aza-Diels–Alder reaction
The aza-Diels–Alder reaction converts imines and dienes to tetrahydropyridines.
New!!: Diels–Alder reaction and Aza-Diels–Alder reaction · See more »
Azomethine ylide
Azomethine ylides are nitrogen-based 1,3-dipoles, consisting of an iminium ion next to a carbanion.
New!!: Diels–Alder reaction and Azomethine ylide · See more »
Barrelene
Barrelene is a bicyclic organic compound with chemical formula C8H8 and systematic name bicycloocta-2,5,7-triene.
New!!: Diels–Alder reaction and Barrelene · See more »
Basketene
Basketene (IUPAC name: pentacyclodec-9-ene) is an organic compound with the formula C10H10.
New!!: Diels–Alder reaction and Basketene · See more »
Bentley compounds
The Bentley compounds are a class of semi-synthetic opioids that were first synthesized by K. W. Bentley by Diels-Alder reaction of thebaine with various dienophiles.
New!!: Diels–Alder reaction and Bentley compounds · See more »
Benzocyclobutadiene
Benzocyclobutadiene is the simplest polycyclic aromatic hydrocarbon, being composed of a benzene ring fused to a cyclobutadiene ring.
New!!: Diels–Alder reaction and Benzocyclobutadiene · See more »
Benzofuran
Benzofuran is the heterocyclic compound consisting of fused benzene and furan rings.
New!!: Diels–Alder reaction and Benzofuran · See more »
Benzylamine
Benzylamine is an organic chemical compound with the condensed structural formula C6H5CH2NH2 (sometimes abbreviated as PhCH2NH2 or BnNH2).
New!!: Diels–Alder reaction and Benzylamine · See more »
Benzylideneacetone
Benzylideneacetone is the organic compound described by the formula C6H5CH.
New!!: Diels–Alder reaction and Benzylideneacetone · See more »
Betaenone B
Betaenone B, like other betaenones (A and C), is a secondary metabolite isolated from the fungus Pleospora betae, a plant pathogen.
New!!: Diels–Alder reaction and Betaenone B · See more »
Biomimetic synthesis
Biomimetic synthesis is an area of organic chemical synthesis that is specifically biologically inspired, so-named in 1917 by the English organic chemist and Nobel laureate Sir Robert Robinson.
New!!: Diels–Alder reaction and Biomimetic synthesis · See more »
Bioorthogonal chemistry
The term bioorthogonal chemistry refers to any chemical reaction that can occur inside of living systems without interfering with native biochemical processes.
New!!: Diels–Alder reaction and Bioorthogonal chemistry · See more »
Bisoxazoline ligand
In chemistry, bis(oxazoline) ligands (often abbreviated BOX ligands) are a class of privileged chiral ligands containing two oxazoline rings.
New!!: Diels–Alder reaction and Bisoxazoline ligand · See more »
Borabenzene
A borabenzene is a heteroaromatic compound that has a boron atom instead of the carbon atom of a benzene molecule.
New!!: Diels–Alder reaction and Borabenzene · See more »
Bradsher cycloaddition
The Bradsher cycloaddition reaction, also known as the Bradsher cyclization reaction is a form of the Diels–Alder reaction which involves the addition of a common dienophile with a cationic aromatic azadiene such as acridizinium or isoquinolinium.
New!!: Diels–Alder reaction and Bradsher cycloaddition · See more »
BTBP
The bis-triazinyl bipyridines (BTBPs) are a class of chemical compounds which are tetradentate ligands similar in shape to quaterpyridine.
New!!: Diels–Alder reaction and BTBP · See more »
Buckminsterfullerene
Buckminsterfullerene is a type of fullerene with the formula C60.
New!!: Diels–Alder reaction and Buckminsterfullerene · See more »
Butyl group
In organic chemistry, butyl is a four-carbon alkyl radical or substituent group with general chemical formula −C4H9, derived from either of the two isomers of butane.
New!!: Diels–Alder reaction and Butyl group · See more »
Captodative effect
The captodative effect is the stabilization of radicals by a synergistic effect of an electron-withdrawing substituent and an electron-donating substituent.
New!!: Diels–Alder reaction and Captodative effect · See more »
Carbon nanotube chemistry
Carbon nanotube chemistry involves chemical reactions, which are used to modify the properties of carbon nanotubes (CNTs).
New!!: Diels–Alder reaction and Carbon nanotube chemistry · See more »
Carbon–carbon bond
A carbon–carbon bond is a covalent bond between two carbon atoms.
New!!: Diels–Alder reaction and Carbon–carbon bond · See more »
Carpanone
Carpanone is a naturally occurring lignan-type natural product most widely known for the remarkably complex way nature prepares it, and the similarly remarkable success that an early chemistry group, that of Orville L. Chapman, had at mimicking nature's pathway.
New!!: Diels–Alder reaction and Carpanone · See more »
CBS catalyst
The CBS catalyst or Corey–Bakshi–Shibata catalyst is an asymmetric catalyst derived from proline.
New!!: Diels–Alder reaction and CBS catalyst · See more »
Chaetoglobosin A
Chaetoglobosin A is a fungal isolate with anticancer activity in vitro.
New!!: Diels–Alder reaction and Chaetoglobosin A · See more »
Cheletropic reaction
Cheletropic reactions Cheletropic reactions also known as chelotropic reactions are a type of pericyclic reaction.
New!!: Diels–Alder reaction and Cheletropic reaction · See more »
Chemical reaction
A chemical reaction is a process that leads to the transformation of one set of chemical substances to another.
New!!: Diels–Alder reaction and Chemical reaction · See more »
Chiral auxiliary
A chiral auxiliary is a stereogenic group or unit that is temporarily incorporated into an organic compound in order to control the stereochemical outcome of the synthesis.
New!!: Diels–Alder reaction and Chiral auxiliary · See more »
Chiral Lewis acid
Chiral Lewis acids (CLAs) are a type of Lewis acid catalyst that effects the chirality of the substrate as it reacts with it.
New!!: Diels–Alder reaction and Chiral Lewis acid · See more »
Chlordane
Chlordane is a chemical compound and also part of a similarly named pesticide mixture resulting from synthesis (main components- heptachlor, chlordane, and nonachlor).
New!!: Diels–Alder reaction and Chlordane · See more »
Chlorendic acid
Chlorendic acid, or 1,4,5,6,7,7-hexachlorobicyclo-hept-5-ene-2,3-dicarboxylic acid, is a chlorinated hydrocarbon used in the synthesis of some flame retardants and polymers.
New!!: Diels–Alder reaction and Chlorendic acid · See more »
Cholesterol total synthesis
Cholesterol total synthesis in chemistry describes the total synthesis of the complex biomolecule cholesterol and is considered a great scientific achievement.
New!!: Diels–Alder reaction and Cholesterol total synthesis · See more »
Christopher Spencer Foote
Christopher Spencer Foote (June 5, 1935 – June 13, 2005) was a professor of chemistry at UCLA and an expert in reactive oxygen species, in particular, singlet oxygen.
New!!: Diels–Alder reaction and Christopher Spencer Foote · See more »
Chromium(III) chloride
Chromium(III) chloride (also called chromic chloride) describes any of several compounds of with the formula CrCl3(H2O)x, where x can be 0, 5, and 6.
New!!: Diels–Alder reaction and Chromium(III) chloride · See more »
Click chemistry
In chemical synthesis, "click" chemistry is a class of biocompatible small molecule reactions commonly used in bioconjugation, allowing the joining of substrates of choice with specific biomolecules.
New!!: Diels–Alder reaction and Click chemistry · See more »
Coarctate reaction
In the classification of organic reactions by transition state topology, a coarctate reaction (from L. coarctare "to constrict") is a third, comparatively uncommon topology, after linear topology and pericyclic topology (itself subdivided into Hückel and Möbius topologies).
New!!: Diels–Alder reaction and Coarctate reaction · See more »
Codinaeopsin
Codinaeopsin is an antimalarial isolated from a fungal isolate found in white yemeri trees (Vochysia guatemalensis) in Costa Rica.
New!!: Diels–Alder reaction and Codinaeopsin · See more »
Copper(II) tetrafluoroborate
Copper(II) tetrafluoroborate is any inorganic compound with the formula Cu(H2O)x(BF4)2.
New!!: Diels–Alder reaction and Copper(II) tetrafluoroborate · See more »
Copper(II) triflate
Copper (II) triflate is the copper(II) salt of trifluoromethanesulfonic acid (known simply as triflic acid) which has a chemical formula of Cu(OSO2CF3)2.
New!!: Diels–Alder reaction and Copper(II) triflate · See more »
Cracking (chemistry)
In petrochemistry, petroleum geology and organic chemistry, cracking is the process whereby complex organic molecules such as kerogens or long-chain hydrocarbons are broken down into simpler molecules such as light hydrocarbons, by the breaking of carbon-carbon bonds in the precursors.
New!!: Diels–Alder reaction and Cracking (chemistry) · See more »
Criegee oxidation
The Criegee oxidation is a glycol cleavage reaction in which vicinal diols are oxidized to form ketones and aldehydes using lead tetraacetate.
New!!: Diels–Alder reaction and Criegee oxidation · See more »
Cubane
Cubane (C8H8) is a synthetic hydrocarbon molecule that consists of eight carbon atoms arranged at the corners of a cube, with one hydrogen atom attached to each carbon atom.
New!!: Diels–Alder reaction and Cubane · See more »
Cyclacene
Cyclacenes are hoop-like polycyclic compounds where aromatic moieties are fused together to form the ring structures.
New!!: Diels–Alder reaction and Cyclacene · See more »
Cyclic compound
A cyclic compound (ring compound) is a term for a compound in the field of chemistry in which one or more series of atoms in the compound is connected to form a ring.
New!!: Diels–Alder reaction and Cyclic compound · See more »
Cycloaddition
A cycloaddition is a pericyclic chemical reaction, in which "two or more unsaturated molecules (or parts of the same molecule) combine with the formation of a cyclic adduct in which there is a net reduction of the bond multiplicity." The resulting reaction is a cyclization reaction.
New!!: Diels–Alder reaction and Cycloaddition · See more »
Cycloalkane
In organic chemistry, the cycloalkanes (also called naphthenes, but distinct from naphthalene) are the monocyclic saturated hydrocarbons.
New!!: Diels–Alder reaction and Cycloalkane · See more »
Cycloalkyne
In organic chemistry, a cycloalkyne is the cyclic analog of an alkyne.
New!!: Diels–Alder reaction and Cycloalkyne · See more »
Cyclobutadiene
Cyclobutadiene is an organic compound with the formula 44.
New!!: Diels–Alder reaction and Cyclobutadiene · See more »
Cyclobutadieneiron tricarbonyl
Cyclobutadieneiron tricarbonyl or (C4H4)Fe(CO)3 is an organoiron compound with the formula Fe(C4H4)(CO)3.
New!!: Diels–Alder reaction and Cyclobutadieneiron tricarbonyl · See more »
Cycloheptatriene
Cycloheptatriene (CHT) is an organic compound with the formula C7H8.
New!!: Diels–Alder reaction and Cycloheptatriene · See more »
Cyclohexene
Cyclohexene is a hydrocarbon with the formula C6H10.
New!!: Diels–Alder reaction and Cyclohexene · See more »
Cyclohexenone
Cyclohexenone is an organic compound which is a versatile intermediate used in the synthesis of a variety of chemical products such as pharmaceuticals and fragrances.
New!!: Diels–Alder reaction and Cyclohexenone · See more »
Cycloisomerization
Cycloisomerization is any isomerization in which the cyclic isomer of the substrate is produced in the reaction coordinate.
New!!: Diels–Alder reaction and Cycloisomerization · See more »
Cyclopentadiene
Cyclopentadiene is an organic compound with the formula C5H6.
New!!: Diels–Alder reaction and Cyclopentadiene · See more »
Cyclopentenone
2-Cyclopentenone is a ketone with chemical formula 56 and CAS number 930-30-3.
New!!: Diels–Alder reaction and Cyclopentenone · See more »
Cyclophane
A cyclophane is a hydrocarbon consisting of an aromatic unit (typically a benzene ring) and an aliphatic chain that forms a bridge between two non-adjacent positions of the aromatic ring.
New!!: Diels–Alder reaction and Cyclophane · See more »
Cyclopropene
Cyclopropene is an organic compound with the formula 34.
New!!: Diels–Alder reaction and Cyclopropene · See more »
Cytochalasin B
Cytochalasin B, the name of which comes from the Greek cytos (cell) and chalasis (relaxation), is a cell-permeable mycotoxin.
New!!: Diels–Alder reaction and Cytochalasin B · See more »
Danishefsky's diene
Danishefsky’s diene (Kitahara diene) is an organosilicon compound and a diene with the formal name trans-1-methoxy-3-trimethylsilyloxy-1,3-butadiene named after Samuel J. Danishefsky.
New!!: Diels–Alder reaction and Danishefsky's diene · See more »
Dechlorane plus
Dechlorane plus (abbrev. DDC-CO) is a polychlorinated flame retardant produced by Oxychem.
New!!: Diels–Alder reaction and Dechlorane plus · See more »
Dendralene
A dendralene is a discrete acyclic cross-conjugated polyene.
New!!: Diels–Alder reaction and Dendralene · See more »
Dendrimer
Dendrimers are repetitively branched molecules.
New!!: Diels–Alder reaction and Dendrimer · See more »
Deoxyribozyme
Deoxyribozymes, also called DNA enzymes, DNAzymes, or catalytic DNA, are DNA oligonucleotides that are capable of performing a specific chemical reaction, often but not always catalytic.
New!!: Diels–Alder reaction and Deoxyribozyme · See more »
Deutzer Friedhof
Deutzer Friedhof is a cemetery in Cologne, Germany.
New!!: Diels–Alder reaction and Deutzer Friedhof · See more »
Dicoronylene
Dicoronylene is the trivial name for a very large polycyclic aromatic hydrocarbon.
New!!: Diels–Alder reaction and Dicoronylene · See more »
Dicyanoacetylene
Dicyanoacetylene, also called carbon subnitride or but-2-ynedinitrile (IUPAC), is a compound of carbon and nitrogen with chemical formula C4N2.
New!!: Diels–Alder reaction and Dicyanoacetylene · See more »
Dicyclopentadiene
Dicyclopentadiene, abbreviated DCPD, is a chemical compound with formula C10H12.
New!!: Diels–Alder reaction and Dicyclopentadiene · See more »
Dieldrin
Dieldrin is an organochloride originally produced in 1948 by J. Hyman & Co, Denver, as an insecticide.
New!!: Diels–Alder reaction and Dieldrin · See more »
Diels
Diels is the last name of several people.
New!!: Diels–Alder reaction and Diels · See more »
Diels–Alder reaction
The Diels–Alder reaction is an organic chemical reaction (specifically, a cycloaddition) between a conjugated diene and a substituted alkene, commonly termed the dienophile, to form a substituted cyclohexene derivative.
New!!: Diels–Alder reaction and Diels–Alder reaction · See more »
Diene
In organic chemistry a diene or diolefin is a hydrocarbon that contains two carbon double bonds.
New!!: Diels–Alder reaction and Diene · See more »
Diethyl azodicarboxylate
Diethyl azodicarboxylate, conventionally abbreviated as DEAD and sometimes as DEADCAT, is an organic compound with the structural formula CH3CH2O2CN.
New!!: Diels–Alder reaction and Diethyl azodicarboxylate · See more »
Diethyl oxomalonate
Diethyl oxomalonate is the diethyl ester of mesoxalic acid (ketomalonic acid), the simplest oxodicarboxylic acid and thus the first member (n.
New!!: Diels–Alder reaction and Diethyl oxomalonate · See more »
Dimer (chemistry)
A dimer (di-, "two" + -mer, "parts") is an oligomer consisting of two monomers joined by bonds that can be either strong or weak, covalent or intermolecular.
New!!: Diels–Alder reaction and Dimer (chemistry) · See more »
Dimethyl acetylenedicarboxylate
Dimethyl acetylenedicarboxylate (DMAD) is an organic compound with the formula CH3O2CC2CO2CH3.
New!!: Diels–Alder reaction and Dimethyl acetylenedicarboxylate · See more »
Dimethyl carbate
Dimethyl carbate is an insect repellent.
New!!: Diels–Alder reaction and Dimethyl carbate · See more »
Dimethylbutadiene
Dimethylbutadiene, formally referred to as 2,3-dimethyl-1,3-butadiene, is an organic compound with the formula (CH3)2C4H4.
New!!: Diels–Alder reaction and Dimethylbutadiene · See more »
Diphosphorus
Diphosphorus is an inorganic chemical with the chemical formula.
New!!: Diels–Alder reaction and Diphosphorus · See more »
Discodermolide
(+)-Discodermolide is a polyketide natural product found to stabilize microtubule.
New!!: Diels–Alder reaction and Discodermolide · See more »
DNA-encoded chemical library
DNA-encoded chemical libraries (DEL) is a technology for the synthesis and screening on unprecedented scale of collections of small molecule compounds.
New!!: Diels–Alder reaction and DNA-encoded chemical library · See more »
Dodecahedrane
Dodecahedrane is a chemical compound (C20H20) first synthesised by Leo Paquette of Ohio State University in 1982, primarily for the "aesthetically pleasing symmetry of the dodecahedral framework".
New!!: Diels–Alder reaction and Dodecahedrane · See more »
Dynamic combinatorial chemistry
Dynamic combinatorial chemistry (DCC); also known as constitutional dynamic chemistry (CDC) is a method to the generation of new molecules formed by reversible reaction of simple building blocks under thermodynamic control.
New!!: Diels–Alder reaction and Dynamic combinatorial chemistry · See more »
Electrocyclic reaction
In organic chemistry, an electrocyclic reaction is a type of pericyclic rearrangement where the net result is one pi bond being converted into one sigma bond or vice versa.
New!!: Diels–Alder reaction and Electrocyclic reaction · See more »
Electronic effect
An electronic effect influences the structure, reactivity, or properties of molecule but is neither a traditional bond nor a steric effect.
New!!: Diels–Alder reaction and Electronic effect · See more »
Elias James Corey
Elias James "E.J." Corey (born July 12, 1928) is an American organic chemist.
New!!: Diels–Alder reaction and Elias James Corey · See more »
Elisabeth Dane
Elisabeth Dane (9 January 1903 – 12 March 1984), was a German biochemist.
New!!: Diels–Alder reaction and Elisabeth Dane · See more »
Endiandric acid C
Endiandric acid C, isolated from the tree Endiandra introrsa, is a well characterized chemical compound.
New!!: Diels–Alder reaction and Endiandric acid C · See more »
Endohedral fullerene
Endohedral fullerenes, also called endofullerenes, are fullerenes that have additional atoms, ions, or clusters enclosed within their inner spheres.
New!!: Diels–Alder reaction and Endohedral fullerene · See more »
Endohedral hydrogen fullerene
Endohedral hydrogen fullerene (H2@C60) is an endohedral fullerene containing molecular hydrogen.
New!!: Diels–Alder reaction and Endohedral hydrogen fullerene · See more »
Endosulfan
Endosulfan is an off-patent organochlorine insecticide and acaricide that is being phased out globally.
New!!: Diels–Alder reaction and Endosulfan · See more »
Ene reaction
The ene reaction (also known as the Alder-ene reaction) is a chemical reaction between an alkene with an allylic hydrogen (the ene) and a compound containing a multiple bond (the enophile), in order to form a new σ-bond with migration of the ene double bond and 1,5 hydrogen shift.
New!!: Diels–Alder reaction and Ene reaction · See more »
Enol ether
An enol ether is an alkene with an alkoxy substituent.
New!!: Diels–Alder reaction and Enol ether · See more »
Enone
An enone, also called an α,β-unsaturated carbonyl, is a type of organic compound consisting of an alkene conjugated to a ketone.
New!!: Diels–Alder reaction and Enone · See more »
Ethyl acrylate
Ethyl acrylate is an organic compound with the formula CH2CHCO2CH2CH3.
New!!: Diels–Alder reaction and Ethyl acrylate · See more »
Ethylidene norbornene
Ethylidene norbornene (ENB) is an organic compound that consists of an ethylene group attached to norbornene.
New!!: Diels–Alder reaction and Ethylidene norbornene · See more »
EuFOD
EuFOD is the chemical compound with the formula Eu(OCC(CH3)3CHCOC3F7)3, also called Eu(fod)3.
New!!: Diels–Alder reaction and EuFOD · See more »
Fencamfamin
Fencamfamin (INN), also known as fencamfamine or by the brand names Glucoenergan and Reactivan, is a stimulant which was developed by Merck in the 1960s.
New!!: Diels–Alder reaction and Fencamfamin · See more »
Foldit
Foldit is an online puzzle video game about protein folding.
New!!: Diels–Alder reaction and Foldit · See more »
Frontier molecular orbital theory
In chemistry, frontier molecular orbital theory is an application of MO theory describing HOMO / LUMO interactions.
New!!: Diels–Alder reaction and Frontier molecular orbital theory · See more »
Fullerene chemistry
Fullerene chemistry is a field of organic chemistry devoted to the chemical properties of fullerenes.
New!!: Diels–Alder reaction and Fullerene chemistry · See more »
Fulvalene
Fulvalene (bicyclopentadienylidene) is the member of the fulvalene family with the molecular formula C10H8.
New!!: Diels–Alder reaction and Fulvalene · See more »
Fumaric acid
Fumaric acid or trans-butenedioic acid is the chemical compound with the formula HO2CCH.
New!!: Diels–Alder reaction and Fumaric acid · See more »
Furan
Furan is a heterocyclic organic compound, consisting of a five-membered aromatic ring with four carbon atoms and one oxygen.
New!!: Diels–Alder reaction and Furan · See more »
Glutaraldehyde
Glutaraldehyde, sold under the brandname Cidex and Glutaral among others, is a disinfectant and medication.
New!!: Diels–Alder reaction and Glutaraldehyde · See more »
Gold(III) bromide
Gold(III) bromide is a dark-red to black crystalline solid.
New!!: Diels–Alder reaction and Gold(III) bromide · See more »
Hagemann's ester
Hagemann's ester, or ethyl-2-methyl-4-oxo-2-cyclohexenecarboxylate, is an organic compound that was first prepared and described in 1893 by German chemist Carl Hagemann.
New!!: Diels–Alder reaction and Hagemann's ester · See more »
Heptacene
Heptacene is an organic compound and a polycyclic aromatic hydrocarbon and the seventh member of the acene or polyacene family of linear fused benzene rings.
New!!: Diels–Alder reaction and Heptacene · See more »
Heptachlor
Heptachlor is an organochlorine compound that was used as an insecticide.
New!!: Diels–Alder reaction and Heptachlor · See more »
Hexabenzocoronene
Hexa-peri-hexabenzocoronene is a polycyclic aromatic hydrocarbon with the molecular formula C42H18.
New!!: Diels–Alder reaction and Hexabenzocoronene · See more »
Hexachlorocyclopentadiene
Hexachlorocyclopentadiene, also known as C-56, is an organochlorine compound that is a precursor to several pesticides.
New!!: Diels–Alder reaction and Hexachlorocyclopentadiene · See more »
Hexadehydro Diels-Alder reaction
In organic chemistry, the hexadehydro-Diels-Alder (HDDA) reaction is an organic chemical reaction between a diyne (2 alkyne functional groups arranged in a conjugated system) and an alkyne to form a reactive benzyne species, via a cycloaddition reaction.
New!!: Diels–Alder reaction and Hexadehydro Diels-Alder reaction · See more »
Hexafluoro-2-butyne
Hexafluoro-2-butyne is the fluorocarbon with the formula CF3C≡CCF3.
New!!: Diels–Alder reaction and Hexafluoro-2-butyne · See more »
Hexafluoroisobutylene
Hexafluoroisobutylene is an organofluorine compound with the formula (CF3)2C.
New!!: Diels–Alder reaction and Hexafluoroisobutylene · See more »
Hexaphenylbenzene
Hexaphenylbenzene is an aromatic compound composed of a benzene ring substituted with six phenyl rings.
New!!: Diels–Alder reaction and Hexaphenylbenzene · See more »
Himbacine
Himbacine is an alkaloid isolated from the bark of Australian magnolias.
New!!: Diels–Alder reaction and Himbacine · See more »
HOMO/LUMO
In chemistry, HOMO and LUMO are types of molecular orbitals.
New!!: Diels–Alder reaction and HOMO/LUMO · See more »
Hydrogen-bond catalysis
Hydrogen-bond catalysis is a type of organocatalysis that relies on use of hydrogen bonding interactions to accelerate and control organic reactions.
New!!: Diels–Alder reaction and Hydrogen-bond catalysis · See more »
Imine Diels–Alder reaction
The imine Diels-Alder reaction involves the transformation of all-carbon dienes and imine dienophiles into tetrahydropyridines.
New!!: Diels–Alder reaction and Imine Diels–Alder reaction · See more »
In-Methylcyclophane
In-Methylcyclophanes are organic compounds and members of a larger family of cyclophanes.
New!!: Diels–Alder reaction and In-Methylcyclophane · See more »
Indenofluorene
Indenofluorenes (IFs) are members of the family of polycyclic hydrocarbons which incorporate a core Indene and a core Fluorene to form a 6-5-6-5-6 ring system.
New!!: Diels–Alder reaction and Indenofluorene · See more »
Indium(III) chloride
Indium(III) chloride is the chemical compound with the formula InCl3.
New!!: Diels–Alder reaction and Indium(III) chloride · See more »
Indole
Indole is an aromatic heterocyclic organic compound with formula C8H7N.
New!!: Diels–Alder reaction and Indole · See more »
Integrasone
Integrasone is a polyketide natural product isolated from an unknown fungus that has been shown the inhibit the HIV-1 integrase enzyme.
New!!: Diels–Alder reaction and Integrasone · See more »
Intramolecular Diels–Alder cycloaddition
In organic chemistry, an intramolecular Diels-Alder cycloaddition is a Diels–Alder reaction in which the diene and a dienophile are both part of the same molecule.
New!!: Diels–Alder reaction and Intramolecular Diels–Alder cycloaddition · See more »
Inverse electron-demand Diels–Alder reaction
The Inverse electron demand Diels–Alder reaction, or DAINV or IEDDA is an organic chemical reaction, in which two new chemical bonds and a six-membered ring are formed.
New!!: Diels–Alder reaction and Inverse electron-demand Diels–Alder reaction · See more »
Ionic liquid
An ionic liquid (IL) is a salt in the liquid state.
New!!: Diels–Alder reaction and Ionic liquid · See more »
Iridoid
Iridoids are a type of monoterpenoids in the general form of cyclopentanopyran, found in a wide variety of plants and some animals.
New!!: Diels–Alder reaction and Iridoid · See more »
Isocyanate
Isocyanate is the functional group with the formula R–N.
New!!: Diels–Alder reaction and Isocyanate · See more »
IUPAC nomenclature for organic transformations
The IUPAC Nomenclature for Transformations is a methodology for naming a chemical reaction.
New!!: Diels–Alder reaction and IUPAC nomenclature for organic transformations · See more »
Jacobsen's catalyst
Jacobsen's catalyst is the common name for N,N'-bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminomanganese(III) chloride, a coordination compound of manganese and a salen-type ligand.
New!!: Diels–Alder reaction and Jacobsen's catalyst · See more »
Kurt Alder
Kurt Alder (10 July 1902 – 20 June 1958) was a German chemist and Nobel laureate.
New!!: Diels–Alder reaction and Kurt Alder · See more »
Lactam
A lactam is a cyclic amide.
New!!: Diels–Alder reaction and Lactam · See more »
Lanthanide trifluoromethanesulfonates
Lanthanide triflates are triflate salts of the lanthanide family with many uses in organic chemistry as Lewis acid catalysts.
New!!: Diels–Alder reaction and Lanthanide trifluoromethanesulfonates · See more »
Lawesson's reagent
Lawesson's reagent, or LR, is a chemical compound used in organic synthesis as a thiation agent.
New!!: Diels–Alder reaction and Lawesson's reagent · See more »
Lewis acid catalysis
In Lewis acid catalysis of organic reactions, a metal-based Lewis acid acts as an electron pair acceptor to increase the reactivity of a substrate.
New!!: Diels–Alder reaction and Lewis acid catalysis · See more »
Limonene
Limonene is a clear, colorless liquid hydrocarbon classified as a cyclic monoterpene, and is the major component in the oil of citrus fruit peels.
New!!: Diels–Alder reaction and Limonene · See more »
Linseed oil
Linseed oil, also known as flaxseed oil or flax oil, is a colourless to yellowish oil obtained from the dried, ripened seeds of the flax plant (Linum usitatissimum).
New!!: Diels–Alder reaction and Linseed oil · See more »
List of German inventions and discoveries
The following (incomplete) list is composed of items, techniques and processes that were invented by or discovered by people from Germany or German-speaking Europe.
New!!: Diels–Alder reaction and List of German inventions and discoveries · See more »
List of German inventors and discoverers
---- This is a list of German inventors and discoverers.
New!!: Diels–Alder reaction and List of German inventors and discoverers · See more »
List of Nobel laureates in Chemistry
The Nobel Prize in Chemistry (Nobelpriset i kemi) is awarded annually by the Royal Swedish Academy of Sciences to scientists in the various fields of chemistry.
New!!: Diels–Alder reaction and List of Nobel laureates in Chemistry · See more »
List of organic reactions
Well-known reactions and reagents in organic chemistry include.
New!!: Diels–Alder reaction and List of organic reactions · See more »
Lithium perchlorate
Lithium perchlorate is the inorganic compound with the formula LiClO4.
New!!: Diels–Alder reaction and Lithium perchlorate · See more »
Lovastatin
Lovastatin (Merck's Mevacor) is a statin drug, used for lowering cholesterol in those with hypercholesterolemia to reduce risk of cardiovascular disease.
New!!: Diels–Alder reaction and Lovastatin · See more »
M. Christina White
M.
New!!: Diels–Alder reaction and M. Christina White · See more »
Macrophomic acid
Macrophomic acid is a fungal metabolite isolated from the fungus Macrophoma commelinae.
New!!: Diels–Alder reaction and Macrophomic acid · See more »
Maleic acid
Maleic acid or cis-butenedioic acid is an organic compound that is a dicarboxylic acid, a molecule with two carboxyl groups.
New!!: Diels–Alder reaction and Maleic acid · See more »
Maleic anhydride
Maleic anhydride is an organic compound with the formula C2H2(CO)2O.
New!!: Diels–Alder reaction and Maleic anhydride · See more »
Maleimide
Maleimide is a chemical compound with the formula H2C2(CO)2NH (see diagram).
New!!: Diels–Alder reaction and Maleimide · See more »
Marshall D. Gates Jr.
Marshall D. Gates Jr. (1915–2003) was an American chemist, holding the position of C.F. Houghton Professor of Chemistry at the University of Rochester.
New!!: Diels–Alder reaction and Marshall D. Gates Jr. · See more »
Mesembrine
Mesembrine is an alkaloid present in Sceletium tortuosum (kanna).
New!!: Diels–Alder reaction and Mesembrine · See more »
Metal-centered cycloaddition reactions
A metal-centered cycloaddition is a subtype of the more general class of cycloaddition reactions.
New!!: Diels–Alder reaction and Metal-centered cycloaddition reactions · See more »
Methyl acrylate
Methyl acrylate is an organic compound, more accurately the methyl ester of acrylic acid.
New!!: Diels–Alder reaction and Methyl acrylate · See more »
Methylcyclopentadiene
Methylcyclopentadiene is any of three isomeric cyclic dialkenes with the formula C5MeH5 (Me.
New!!: Diels–Alder reaction and Methylcyclopentadiene · See more »
Methylene blue
Methylene blue, also known as methylthioninium chloride, is a medication and dye.
New!!: Diels–Alder reaction and Methylene blue · See more »
Mevastatin
Mevastatin (compactin, ML-236B) is a hypolipidemic agent that belongs to the statins class.
New!!: Diels–Alder reaction and Mevastatin · See more »
Michael E. Jung
Michael E. Jung is a Professor of Chemistry in the Department of Chemistry and Biochemistry at the University of California at Los Angeles.
New!!: Diels–Alder reaction and Michael E. Jung · See more »
Montréalone
Montréalone (synonyms: montrealone, phospha-münchnone) is a mesoionic heterocyclic chemical compound.
New!!: Diels–Alder reaction and Montréalone · See more »
Myrcene
Myrcene, or β-myrcene, is an olefinic natural organic hydrocarbon.
New!!: Diels–Alder reaction and Myrcene · See more »
Myrcenol
Myrcenol is an organic compound, specifically a terpenoid.
New!!: Diels–Alder reaction and Myrcenol · See more »
N-Sulfinylaniline
N-Sulfinylaniline is the organosulfur compound with the formula C6H5NSO.
New!!: Diels–Alder reaction and N-Sulfinylaniline · See more »
Name reaction
A name reaction is a chemical reaction named after its discoverers or developers.
New!!: Diels–Alder reaction and Name reaction · See more »
Naphthalene
Naphthalene is an organic compound with formula.
New!!: Diels–Alder reaction and Naphthalene · See more »
Neighbouring group participation
Neighbouring group participation (NGP) (also known as anchimeric assistance) in organic chemistry has been defined by IUPAC as the interaction of a reaction centre with a lone pair of electrons in an atom or the electrons present in a sigma bond or pi bond contained within the parent molecule but not conjugated with the reaction centre.
New!!: Diels–Alder reaction and Neighbouring group participation · See more »
Nicolaou Taxol total synthesis
The Nicolaou Taxol total synthesis, published by K. C. Nicolaou and his group in 1994 concerns the total synthesis of Taxol.
New!!: Diels–Alder reaction and Nicolaou Taxol total synthesis · See more »
Niobium(V) chloride
Niobium(V) chloride, also known as niobium pentachloride, is a yellow crystalline solid.
New!!: Diels–Alder reaction and Niobium(V) chloride · See more »
Nitroalkene
A nitroalkene, or nitro olefin, is a functional group combining the functionality of its constituent parts, an alkene and nitro group, while displaying its own chemical properties through alkene activation, making the functional group useful in specialty reactions such as the Michael reaction or Diels-Alder additions.
New!!: Diels–Alder reaction and Nitroalkene · See more »
Nitrosobenzene
Nitrosobenzene is the organic compound with the formula C6H5NO.
New!!: Diels–Alder reaction and Nitrosobenzene · See more »
Norbadione A
Norbadione A is a pigment found in the bay bolete mushroom (Boletus badius).
New!!: Diels–Alder reaction and Norbadione A · See more »
Norbornadiene
Norbornadiene is a bicyclic hydrocarbon and an organic compound.
New!!: Diels–Alder reaction and Norbornadiene · See more »
Norbornene
Norbornene or norbornylene or norcamphene is a bridged cyclic hydrocarbon.
New!!: Diels–Alder reaction and Norbornene · See more »
Nosiheptide
Nosiheptide is a thiopeptide antibiotic produced by the bacterium Streptomyces actuosus.
New!!: Diels–Alder reaction and Nosiheptide · See more »
On water reaction
On water reactions are a group of organic reactions that take place as an emulsion in water and that exhibit an unusual reaction rate acceleration compared to the same reaction in an organic solvent or compared to the corresponding dry media reaction.
New!!: Diels–Alder reaction and On water reaction · See more »
Organic acid anhydride
An organic acid anhydride is an acid anhydride that is an organic compound.
New!!: Diels–Alder reaction and Organic acid anhydride · See more »
Organic reaction
Organic reactions are chemical reactions involving organic compounds.
New!!: Diels–Alder reaction and Organic reaction · See more »
Organocatalysis
In organic chemistry, the term organocatalysis (a portmanteau of the terms "organic" and "catalyst") refers to a form of catalysis, whereby the rate of a chemical reaction is increased by an organic catalyst referred to as an "organocatalyst" consisting of carbon, hydrogen, sulfur and other nonmetal elements found in organic compounds.
New!!: Diels–Alder reaction and Organocatalysis · See more »
Organogold chemistry
Organogold chemistry is the study of compounds containing gold–carbon bonds.
New!!: Diels–Alder reaction and Organogold chemistry · See more »
Organoiron chemistry
Organoiron chemistry is the chemistry of iron compounds containing a carbon-to-iron chemical bond.
New!!: Diels–Alder reaction and Organoiron chemistry · See more »
Oripavine
Oripavine is an opiate and the major metabolite of thebaine.
New!!: Diels–Alder reaction and Oripavine · See more »
Oseltamivir total synthesis
Oseltamivir total synthesis concerns the total synthesis of the antiinfluenza drug oseltamivir marketed by Hoffmann-La Roche under the trade name Tamiflu.
New!!: Diels–Alder reaction and Oseltamivir total synthesis · See more »
Otto Diels
Otto Paul Hermann Diels (23 January 1876 – 7 March 1954) was a German chemist.
New!!: Diels–Alder reaction and Otto Diels · See more »
Outline of organic chemistry
The following outline is provided as an overview of and topical guide to organic chemistry: Organic chemistry – scientific study of the structure, properties, composition, reactions, and preparation (by synthesis or by other means) of carbon-based compounds, hydrocarbons, and their derivatives.
New!!: Diels–Alder reaction and Outline of organic chemistry · See more »
Oxanorbornadiene
Oxanorbornadiene (OND) is a bicyclic organic compound with an oxygen atom bridging the two opposing saturated carbons of 1,4-cyclohexadiene.
New!!: Diels–Alder reaction and Oxanorbornadiene · See more »
Oxazole
Oxazole is the parent compound for a vast class of heterocyclic aromatic organic compounds.
New!!: Diels–Alder reaction and Oxazole · See more »
Oxo-Diels–Alder reaction
An oxo-Diels–Alder reaction (also called an oxa-Diels–Alder reaction) is an organic reaction and a variation of the Diels–Alder reaction in which a suitable diene reacts with an aldehyde to form a dihydropyran ring.
New!!: Diels–Alder reaction and Oxo-Diels–Alder reaction · See more »
Oxocarbenium
An oxocarbenium ion (or oxacarbenium ion) is a chemical species characterized by a central sp2-hybridized carbon, an oxygen substituent, and an overall positive charge that is delocalized between the central carbon and oxygen atoms.
New!!: Diels–Alder reaction and Oxocarbenium · See more »
Phosphaalkene
Phosphaalkenes (IUPAC name: alkylidenephosphanes) are organophosphorus compounds with double bonds between carbon and phosphorus(III) with the formula R2C.
New!!: Diels–Alder reaction and Phosphaalkene · See more »
Phosphole
Phosphole is the organic compound with the chemical formula C4H4PH; it is the phosphorus analog of pyrrole.
New!!: Diels–Alder reaction and Phosphole · See more »
Photochemistry
Photochemistry is the branch of chemistry concerned with the chemical effects of light.
New!!: Diels–Alder reaction and Photochemistry · See more »
Photoredox catalysis
Photoredox catalysis is a branch of catalysis that harnesses the energy of light to accelerate a chemical reaction via single-electron transfer events.
New!!: Diels–Alder reaction and Photoredox catalysis · See more »
Physical organic chemistry
Physical organic chemistry, a term coined by Louis Hammett in 1940, refers to a discipline of organic chemistry that focuses on the relationship between chemical structures and reactivity, in particular, applying experimental tools of physical chemistry to the study of organic molecules.
New!!: Diels–Alder reaction and Physical organic chemistry · See more »
Podophyllotoxin
Podophyllotoxin (PPT), also known as podofilox, is a medical cream that is used to treat genital warts and molluscum contagiosum.
New!!: Diels–Alder reaction and Podophyllotoxin · See more »
Polyacetylene
Polyacetylene (IUPAC name: polyethyne) usually refers to an organic polymer with the repeating unit (C2H2)n.
New!!: Diels–Alder reaction and Polyacetylene · See more »
Potential applications of graphene
Potential graphene applications include lightweight, thin, flexible, yet incredibly lightweight to, electric/photonics circuits, solar cells, and various medical, chemical and industrial processes enhanced or enabled by the use of new graphene materials.
New!!: Diels–Alder reaction and Potential applications of graphene · See more »
Prato reaction
The Prato reaction is a particular example of the well-known 1,3-dipolar cycloaddition of azomethine ylides to olefins.
New!!: Diels–Alder reaction and Prato reaction · See more »
PRIME (PRobe Incorporation Mediated by Enzymes)
PRIME (PRobe Incorporation Mediated by Enzymes) is a molecular biology research tool developed by Alice Y. Ting and the Ting Lab at MIT for site-specific labeling of proteins in living cells with chemical probes.
New!!: Diels–Alder reaction and PRIME (PRobe Incorporation Mediated by Enzymes) · See more »
Prismane
Prismane or 'Ladenburg benzene' is a polycyclic hydrocarbon with the formula C6H6.
New!!: Diels–Alder reaction and Prismane · See more »
Process chemistry
Process chemistry is the arm of pharmaceutical chemistry concerned with the development and optimization of a synthetic scheme and pilot plant procedure to manufacture compounds for the drug development phase.
New!!: Diels–Alder reaction and Process chemistry · See more »
Protein design
Protein design is the rational design of new protein molecules to design novel activity, behavior, or purpose, and to advance basic understanding of protein function.
New!!: Diels–Alder reaction and Protein design · See more »
Pyramidal alkene
Pyramidal alkenes are alkenes in which the two carbon atoms making up the double bond are not coplanar with their four substituents.
New!!: Diels–Alder reaction and Pyramidal alkene · See more »
Pyrene
Pyrene is a polycyclic aromatic hydrocarbon (PAH) consisting of four fused benzene rings, resulting in a flat aromatic system.
New!!: Diels–Alder reaction and Pyrene · See more »
Pyrrole
Pyrrole is a heterocyclic aromatic organic compound, a five-membered ring with the formula C4H4NH.
New!!: Diels–Alder reaction and Pyrrole · See more »
Pyrylium salt
The pyrylium cation is a six-membered, unsaturated, mono-cyclic compound.
New!!: Diels–Alder reaction and Pyrylium salt · See more »
Quaternary carbon
A quaternary carbon is a carbon atom bound to four other carbon atoms.
New!!: Diels–Alder reaction and Quaternary carbon · See more »
Retro-Diels–Alder reaction
The retro-Diels–Alder reaction (rDA) is the microscopic reverse of the Diels–Alder reaction—the formation of a diene and dienophile from a cyclohexene.
New!!: Diels–Alder reaction and Retro-Diels–Alder reaction · See more »
Ring forming reaction
A ring forming reaction or ring-closing reaction in organic chemistry is a general term for a variety of reactions that introduce one or more rings into a molecule.
New!!: Diels–Alder reaction and Ring forming reaction · See more »
Robert Burns Woodward
Robert Burns Woodward (April 10, 1917 – July 8, 1979) was an American organic chemist.
New!!: Diels–Alder reaction and Robert Burns Woodward · See more »
Rubicordifolin
Rubicordifolin is a natural product that is produced by Rubia cordifolia, a plant that is a member of the Rubiaceae family.
New!!: Diels–Alder reaction and Rubicordifolin · See more »
Rubottom oxidation
The Rubottom oxidation is a useful, high-yielding chemical reaction between silyl enol ethers and peroxyacids to give the corresponding α-hydroxy carbonyl product.
New!!: Diels–Alder reaction and Rubottom oxidation · See more »
RXNO Ontology
The RXNO Ontology is a formal ontology of chemical named reactions.
New!!: Diels–Alder reaction and RXNO Ontology · See more »
Saegusa–Ito oxidation
The Saegusa–Ito oxidation is a chemical reaction used in organic chemistry.
New!!: Diels–Alder reaction and Saegusa–Ito oxidation · See more »
Salvinorin A
Salvinorin A is the main active psychotropic molecule in Salvia divinorum, a Mexican plant which has a long history of use as an entheogen by indigenous Mazatec shamans.
New!!: Diels–Alder reaction and Salvinorin A · See more »
Scientific phenomena named after people
This is a list of scientific phenomena and concepts named after people (eponymous phenomena).
New!!: Diels–Alder reaction and Scientific phenomena named after people · See more »
Self-healing material
Self-healing materials are artificial or synthetically-created substances that have the built-in ability to automatically repair damage to themselves without any external diagnosis of the problem or human intervention.
New!!: Diels–Alder reaction and Self-healing material · See more »
Shibasaki catalysts
Shibasaki catalysts are a class of hetero-bimetallic complexes with the general formula (M.
New!!: Diels–Alder reaction and Shibasaki catalysts · See more »
Silabenzene
A silabenzene is a heteroaromatic compound containing one or more silicon atoms instead of carbon atoms in benzene.
New!!: Diels–Alder reaction and Silabenzene · See more »
Silsesquioxane
A cubic silsesquioxane. A silsesquioxane is an organosilicon compound with the chemical formula n (R.
New!!: Diels–Alder reaction and Silsesquioxane · See more »
Singlet oxygen
Singlet oxygen, systematically named dioxygen(singlet) and dioxidene, is a gaseous inorganic chemical with the formula O.
New!!: Diels–Alder reaction and Singlet oxygen · See more »
Stannabenzene
Stannabenzene (C5H6Sn) is the parent representative of a group of organotin compounds that are related to benzene with a carbon atom replaced by a tin atom.
New!!: Diels–Alder reaction and Stannabenzene · See more »
Stereoelectronic effect
The stereoelectronic effect is the effect on molecular structures, physical properties and reactivities due to the molecules' electronic structures, in particular the interaction between atomic and/or molecular orbitals.
New!!: Diels–Alder reaction and Stereoelectronic effect · See more »
Stereospecificity
In chemistry, stereospecificity is the property of a reaction mechanism that leads to different stereoisomeric reaction products from different stereoisomeric reactants, or which operates on only one (or a subset) of the stereoisomers.
New!!: Diels–Alder reaction and Stereospecificity · See more »
Stille reaction
The Stille reaction, or the Migita–Kosugi–Stille coupling, is a chemical reaction widely used in organic synthesis which involves the coupling of an organotin compound (also known as organostannanes) with a variety of organic electrophiles via palladium-catalyzed coupling reaction.
New!!: Diels–Alder reaction and Stille reaction · See more »
Strychnine total synthesis
Strychnine total synthesis in chemistry describes the total synthesis of the complex biomolecule strychnine.
New!!: Diels–Alder reaction and Strychnine total synthesis · See more »
Sulfene
Sulfene is an extremely reactive chemical compound with the formula H2C.
New!!: Diels–Alder reaction and Sulfene · See more »
Sulfolene
Sulfolene, or butadiene sulfone is a cyclic organic chemical with a sulfone functional group.
New!!: Diels–Alder reaction and Sulfolene · See more »
Sulfur diimide
Sulfur diimides are chemical compounds of the formula S(NR)2.
New!!: Diels–Alder reaction and Sulfur diimide · See more »
Supramolecular catalysis
Supramolecular catalysis is not a well-defined field but it generally refers to an application of supramolecular chemistry, especially molecular recognition and guest binding, toward catalysis.
New!!: Diels–Alder reaction and Supramolecular catalysis · See more »
Tetrahydrobenzaldehyde
1,2,3,6-Tetrahydrobenzaldehyde is an organic compound with the formula C6H9CHO.
New!!: Diels–Alder reaction and Tetrahydrobenzaldehyde · See more »
Tetrahydrophthalic anhydride
Tetrahydrophthalic anhydride is an organic compound with the formula C6H8C2O3.
New!!: Diels–Alder reaction and Tetrahydrophthalic anhydride · See more »
Tetramethyl acetyloctahydronaphthalenes
No description.
New!!: Diels–Alder reaction and Tetramethyl acetyloctahydronaphthalenes · See more »
Tetraphenylcyclopentadienone
Tetraphenylcyclopentadienone is an organic compound with the formula (C6H5)4C4CO.
New!!: Diels–Alder reaction and Tetraphenylcyclopentadienone · See more »
Tetrazine
Tetrazine is an unstable compound that consists of a six-membered aromatic ring containing four nitrogen atoms with the molecular formula C2H2N4.
New!!: Diels–Alder reaction and Tetrazine · See more »
Tetrodotoxin
Tetrodotoxin (TTX) is a potent neurotoxin.
New!!: Diels–Alder reaction and Tetrodotoxin · See more »
Thermal scanning probe lithography
Thermal scanning probe lithography (t-SPL) is a form of scanning probe lithography (SPL) whereby material is structured on the nanoscale using scanning probes, primarily through the application of thermal energy. Related fields are thermo-mechanical SPL (see also Millipede memory), thermochemical SPL (or thermochemical nanolithography) where the goal is to influence the local chemistry, and thermal Dip Pen Lithography as an additive technique.
New!!: Diels–Alder reaction and Thermal scanning probe lithography · See more »
Thermodynamic versus kinetic reaction control
Thermodynamic reaction control or kinetic reaction control in a chemical reaction can decide the composition in a reaction product mixture when competing pathways lead to different products and the reaction conditions influence the selectivity or stereoselectivity.
New!!: Diels–Alder reaction and Thermodynamic versus kinetic reaction control · See more »
Thial
A thial or thioaldehyde is a functional group in organic chemistry which is similar to an aldehyde, RC(O)H, in which a sulfur (S) atom replaces the oxygen (O) atom of the aldehyde (R represents an alkyl or aryl group).
New!!: Diels–Alder reaction and Thial · See more »
Thiazole
Thiazole, or 1,3-thiazole, is a heterocyclic compound that contains both sulfur and nitrogen; the term 'thiazole' also refers to a large family of derivatives.
New!!: Diels–Alder reaction and Thiazole · See more »
Thiobenzophenone
Thiobenzophenone is an organosulfur compound with the formula (C6H5)2CS.
New!!: Diels–Alder reaction and Thiobenzophenone · See more »
Thioketone
Thioketones (also known as thiones or thiocarbonyls) are organosulfur compounds related to conventional ketones.
New!!: Diels–Alder reaction and Thioketone · See more »
Thiophene
Thiophene is a heterocyclic compound with the formula C4H4S.
New!!: Diels–Alder reaction and Thiophene · See more »
Thiophosgene
Thiophosgene is a red liquid with the formula CSCl2.
New!!: Diels–Alder reaction and Thiophosgene · See more »
Tilidine
Tilidine, or tilidate (brand names: Tilidin, Valoron and Valtran) is a synthetic opioid painkiller, used mainly in Germany, Switzerland, South Africa and Belgium for treatment of moderate to severe pain, both acute and chronic.
New!!: Diels–Alder reaction and Tilidine · See more »
Timeline of biology and organic chemistry
Significant events in biology and organic chemistry.
New!!: Diels–Alder reaction and Timeline of biology and organic chemistry · See more »
Torreyanic acid
Torreyanic acid is a dimeric quinone first isolated and by Lee et al. in 1996 from an endophyte, Pestalotiopsis microspora.
New!!: Diels–Alder reaction and Torreyanic acid · See more »
Total synthesis of morphine and related alkaloids
Synthesis of morphine-like alkaloids in chemistry describes the total synthesis of the natural morphinan class of alkaloids that includes codeine, morphine, oripavine, and thebaine and the closely related semisynthetic analogs buprenorphine, hydrocodone, isocodeine, naltrexone, naloxone, nalbuphine, and oxycodone.
New!!: Diels–Alder reaction and Total synthesis of morphine and related alkaloids · See more »
Triazine
A triazine is class of nitrogen-containing heterocycles.
New!!: Diels–Alder reaction and Triazine · See more »
Tricyclobutabenzene
Tricyclobutabenzene is an aromatic hydrocarbon consisting of a benzene core with three cyclobutane rings fused onto it.
New!!: Diels–Alder reaction and Tricyclobutabenzene · See more »
Triflate
Triflate, also known by the systematic name trifluoromethanesulfonate, is a functional group with the formula CF3SO3−.
New!!: Diels–Alder reaction and Triflate · See more »
Trifluoroperacetic acid
Trifluoroperacetic acid (trifluoroperoxyacetic acid, TFPAA) is the peroxy acid analog of trifluoroacetic acid and has the condensed structural formula.
New!!: Diels–Alder reaction and Trifluoroperacetic acid · See more »
Trimetasphere
Trimetasphere carbon nanomaterials (TMS), also known as trimetallic nitride endohedral metallofullerenes, are a family of endohedral metallofullerenes (EMF).
New!!: Diels–Alder reaction and Trimetasphere · See more »
Tripamide
Tripamide (INN) is a diuretic.
New!!: Diels–Alder reaction and Tripamide · See more »
Triptycene
Triptycene is an aromatic hydrocarbon, the simplest iptycene molecule with the formula C2H2(C6H4)3.
New!!: Diels–Alder reaction and Triptycene · See more »
Tropone
Tropone or 2,4,6-cycloheptatrien-1-one is an organic compound with some importance in organic chemistry as a non-benzenoid aromatic.
New!!: Diels–Alder reaction and Tropone · See more »
Ugi reaction
The Ugi reaction is a multi-component reaction in organic chemistry involving a ketone or aldehyde, an amine, an isocyanide and a carboxylic acid to form a bis-amide.
New!!: Diels–Alder reaction and Ugi reaction · See more »
Umpolung
Umpolung or polarity inversion in organic chemistry is the chemical modification of a functional group with the aim of the reversal of polarity of that group.
New!!: Diels–Alder reaction and Umpolung · See more »
Vicinal difunctionalization
Vicinal difunctionalization refers to a chemical reaction involving transformations at two adjacent centers (most commonly carbons).
New!!: Diels–Alder reaction and Vicinal difunctionalization · See more »
Vinyl acetate
Vinyl acetate is an organic compound with the formula CH3CO2CH.
New!!: Diels–Alder reaction and Vinyl acetate · See more »
Vinyl norbornene
Vinyl norbornene (VNB) is an organic compound that consists of a vinyl group attached to norbornene.
New!!: Diels–Alder reaction and Vinyl norbornene · See more »
Vinylcyclopropane rearrangement
The vinylcyclopropane rearrangement or vinylcyclopropane-cyclopentene rearrangement is a ring expansion reaction, converting a vinyl-substituted cyclopropane ring into a cyclopentene ring.
New!!: Diels–Alder reaction and Vinylcyclopropane rearrangement · See more »
Vinyldithiin
Vinyldithiins, more precisely named 3-vinyl-4H-1,2-dithiin and 2-vinyl-4H-1,3-dithiin, are organosulfur phytochemicals formed in the breakdown of allicin from crushed garlic (Allium sativum).
New!!: Diels–Alder reaction and Vinyldithiin · See more »
Vinylene carbonate
Vinylene carbonate (VC) or 1,3-dioxol-2-one, is the simplest unsaturated cyclic carbonic acid ester.
New!!: Diels–Alder reaction and Vinylene carbonate · See more »
Vitamin B12 total synthesis
The total synthesis of the complex biomolecule vitamin B12 was first accomplished by the collaborating research groups of Robert Burns Woodward at Harvard and Albert Eschenmoser at ETH in 1972.
New!!: Diels–Alder reaction and Vitamin B12 total synthesis · See more »
Wagner-Jauregg reaction
The Wagner-Jauregg reaction is a classic organic reaction in organic chemistry, named after Theodor Wagner-Jauregg, describing the double Diels–Alder reaction of 2 equivalents of maleic anhydride with a 1,1-diarylethylene.
New!!: Diels–Alder reaction and Wagner-Jauregg reaction · See more »
Water
Water is a transparent, tasteless, odorless, and nearly colorless chemical substance that is the main constituent of Earth's streams, lakes, and oceans, and the fluids of most living organisms.
New!!: Diels–Alder reaction and Water · See more »
William R. Roush
William R. Roush is an American organic chemist.
New!!: Diels–Alder reaction and William R. Roush · See more »
Woodward–Hoffmann rules
The Woodward–Hoffmann rules (or the pericyclic selection rules), devised by Robert Burns Woodward and Roald Hoffmann, are a set of rules used to rationalize or predict certain aspects of the stereochemical outcome and activation energy of pericyclic reactions, an important class of reactions in organic chemistry.
New!!: Diels–Alder reaction and Woodward–Hoffmann rules · See more »
Ytterbium
Ytterbium is a chemical element with symbol Yb and atomic number 70.
New!!: Diels–Alder reaction and Ytterbium · See more »
Yuehchukene
Yuehchukene is a dimeric indole alkaloid natural product that possesses anti-fertility and estrogenic activities.
New!!: Diels–Alder reaction and Yuehchukene · See more »
Zirconium(IV) chloride
Zirconium(IV) chloride, also known as zirconium tetrachloride, is an inorganic compound frequently used as a precursor to other compounds of zirconium.
New!!: Diels–Alder reaction and Zirconium(IV) chloride · See more »
1,2,3,4-Tetraphenylnaphthalene
1,2,3,4-Tetraphenylnaphthalene is a polycyclic aromatic hydrocarbon commonly prepared in the undergraduate teaching laboratory as an introduction to the Diels-Alder reaction, in this case between benzyne, which acts as the dienophile, (generated in situ) and tetraphenylcyclopentadienone, which acts as the diene.
New!!: Diels–Alder reaction and 1,2,3,4-Tetraphenylnaphthalene · See more »
1,2,4,5-Tetrabromobenzene
1,2,4,5-Tetrabromobenzene is a fourfold symmetrically bromine-substituted benzene and starting material for liquid crystals and OLED materials, as well as for mono- and bis-aryines.
New!!: Diels–Alder reaction and 1,2,4,5-Tetrabromobenzene · See more »
1,2-Cyclohexane dicarboxylic acid diisononyl ester
1,2-Cyclohexane dicarboxylic acid diisononyl ester is a plasticizer for the manufacture of flexible plastic articles in sensitive application areas such as toys, medical devices and food packaging.
New!!: Diels–Alder reaction and 1,2-Cyclohexane dicarboxylic acid diisononyl ester · See more »
1,3-Butadiene
1,3-Butadiene is the organic compound with the formula (CH2.
New!!: Diels–Alder reaction and 1,3-Butadiene · See more »
1,3-Cyclohexadiene
1,3-Cyclohexadiene is an organic compound with the formula (CH2)2(CH)4.
New!!: Diels–Alder reaction and 1,3-Cyclohexadiene · See more »
1,3-Dipolar cycloaddition
The 1,3-dipolar cycloaddition is a chemical reaction between a 1,3-dipole and a dipolarophile to form a five-membered ring.
New!!: Diels–Alder reaction and 1,3-Dipolar cycloaddition · See more »
1,4-Benzoquinone
1,4-Benzoquinone, commonly known as para-quinone, is a chemical compound with the formula C6H4O2.
New!!: Diels–Alder reaction and 1,4-Benzoquinone · See more »
1,4-Dioxin
1,4-Dioxin (also referred as dioxin or p-dioxin) is a heterocyclic, organic, non-aromatic compound with the chemical formula C4H4O2.
New!!: Diels–Alder reaction and 1,4-Dioxin · See more »
1,4-Naphthoquinone
1,4-Naphthoquinone or para-naphthoquinone is an organic compound derived from naphthalene.
New!!: Diels–Alder reaction and 1,4-Naphthoquinone · See more »
1,7-Octadiene
1,7-Octadiene (C8H14) is a light flammable organic compound.
New!!: Diels–Alder reaction and 1,7-Octadiene · See more »
1928 in science
The year 1928 in science and technology involved some significant events, listed below.
New!!: Diels–Alder reaction and 1928 in science · See more »
2,5-Dimethylfuran
2,5-Dimethylfuran is a heterocyclic compound with the formula (CH3)2C4H2O.
New!!: Diels–Alder reaction and 2,5-Dimethylfuran · See more »
2-Pyrone
2-Pyrone (α-pyrone or pyran-2-one) is an unsaturated cyclic chemical compound with the molecular formula C5H4O2.
New!!: Diels–Alder reaction and 2-Pyrone · See more »
3-Bromofuran
3-Bromofuran is a liquid having a boiling point similar to that of water (102.5-102.6 °C), but with density significantly higher (1.6606 g/cm3 at 20 °C).
New!!: Diels–Alder reaction and 3-Bromofuran · See more »
4+3 cycloaddition
A Cycloaddition is a cycloaddition between a 4 atom pi-system and a 3 atom pi-system to form a seven-membered ring.
New!!: Diels–Alder reaction and 4+3 cycloaddition · See more »
4,7-Dihydroisoindole
4,7-Dihydroisoindole in heterocyclic chemistry is a reduced form of isoindole.
New!!: Diels–Alder reaction and 4,7-Dihydroisoindole · See more »
4-Phenyl-1,2,4-triazole-3,5-dione
4-Phenyl-1,2,4-triazoline-3,5-dione (PTAD) is an azodicarbonyl compound.
New!!: Diels–Alder reaction and 4-Phenyl-1,2,4-triazole-3,5-dione · See more »
4-Vinylcyclohexene
4-Vinylcyclohexene is an organic compound formed when 1,3-butadiene dimerizes in a Diels-Alder reaction.
New!!: Diels–Alder reaction and 4-Vinylcyclohexene · See more »
Redirects here:
Alder-Stein rules, Alder–Stein rules, Asymmetric Diels-Alder reaction, Diels Alder, Diels Alder reaction, Diels alders reaction, Diels-Adler reaction, Diels-Alder, Diels-Alder Reaction, Diels-Alder addition, Diels-Alder cyclization, Diels-Alder cycloaddition reaction, Diels-Alder reaction, Diels-Alder reactions, Diels–Alder, Diene synthesis, Dienophile, Endo Rule, Endo rule, Retro Diels Alder, Retro Diels–Alder reaction, Rickert-Alder reaction, Synthesen in der hydroaromatischen Reihe.
References
[1] https://en.wikipedia.org/wiki/Diels–Alder_reaction
