200 relations: Alan J. Heeger, Aldol condensation, Aldol reaction, Alkyl nitrites, Alkyne metathesis, Allylic rearrangement, Andrew Bruce Holmes, Aromatization, Azide-alkyne Huisgen cycloaddition, Baldwin's rules, Barton decarboxylation, Barton–McCombie deoxygenation, Beckmann rearrangement, Ben Feringa, Beta-peptide, Biaxial nematic, Bis(cyclopentadienyl)titanium(III) chloride, Cambridge Structural Database, Carbene dye, Carbon nanotube, Carroll rearrangement, CBS catalyst, Chemical glycosylation, Chemical Science (journal), Cluster chemistry, Cobalt(II) chloride, Colin Raston, Copper(II) bromide, Corey–Itsuno reduction, Crabtree's catalyst, CrystEngComm, CrystEngCommunity, Cucurbituril, David Klenerman, Dendrimer, Dewar benzene, Di-tert-butyl dicarbonate, Di-tert-butyl peroxide, Dianin's compound, Diarylethene, Diborane(2), Dicarbonyltris(triphenylphosphine)ruthenium(0), Dieter Seebach, Diethylamine, Dimethylcadmium, Directed ortho metalation, Don Tilley, Donald E. Pearson, Douglas C. Gordon, Electron affinity, ..., Enyne metathesis, Ferrier carbocyclization, Ferrocene, Finkelstein reaction, Fleming–Tamao oxidation, Fluoroantimonic acid, Four-center two-electron bond, Gautam Radhakrishna Desiraju, Glutaconaldehyde, Graphyne, Hajos–Parrish–Eder–Sauer–Wiechert reaction, Halogenation, Halonium ion, Hantzsch pyrrole synthesis, Hauser base, Hückel's rule, Heck reaction, Henry Rzepa, Hexol, High-temperature superconductivity, Hofmann–Löffler reaction, Homochirality, Horner–Wadsworth–Emmons reaction, Hydrazine, Hydrazone iodination, Hydrocyanation, Hydroxylamine-O-sulfonic acid, Intramolecular reaction, Iodane, Iodosobenzene, Ionic liquid, Irshad Hussain, Isomer, Isomerization, Johnson–Corey–Chaykovsky reaction, Journal of the Chemical Society, Juliá–Colonna epoxidation, Krogmann's salt, Lanthanide trifluoromethanesulfonates, Lawesson's reagent, Lead, Lead(II) nitrate, List of chemistry journals, List of Royal Society of Chemistry journals, List of scientific journals, Lithium nitride, Luche reduction, Markó–Lam deoxygenation, Martin A. Bennett, Mauveine, Mechanically interlocked molecular architectures, Metal acetylacetonates, Metal aromaticity, Metal–organic framework, Metallabenzene, Microreactor, Molecular Borromean rings, Murchison meteorite, N-Chlorosuccinimide, Nanofiber seeding, Nazarov cyclization reaction, Nitrile, Nitrilimine, Nitrogen, Nitrone-olefin (3+2) cycloaddition, Noble gas compound, On water reaction, Organic and Biomolecular Chemistry, Organocadmium compound, Organonickel, Organopalladium, Organophosphorus compound, Organosilicon, Organotellurium chemistry, Osmium(IV) chloride, Oxazole, P4-t-Bu, Paal–Knorr synthesis, Paclitaxel total synthesis, Paolo Samorì, Paramasivam Natarajan, Pentacene, Pentamethylcyclopentadiene, Pentamethylcyclopentadienyl rhodium dichloride dimer, Peptide synthesis, Persistent carbene, Peter Maitlis, Phase-boundary catalysis, Phenylacetylene, Phenylboronic acid, Phosphonium, Phosphorus triiodide, Pi bond, PMDTA, Polymorphism (materials science), Pummerer rearrangement, Pyrylium salt, Quintuple bond, Radon, Radon difluoride, Ramberg–Bäcklund reaction, Resorcinarene, Roger Alder, Rotaxane, Royal Society of Chemistry, RSC Advances, Saegusa–Ito oxidation, Salt bridge (protein and supramolecular), Sandeep Verma, Sandwich compound, Schwartz's reagent, Sigmatropic reaction, Silver acetylide, Single-molecule magnet, Solubility, Sonogashira coupling, Sumanene, Supercritical fluid, Supramolecular catalysis, Supramolecular electronics, Synthetic setae, Taxodone, Tert-Butyloxycarbonyl protecting group, Tetramethylurea, Tetrapropylammonium perruthenate, Thiazole, Thin-layer chromatography, Titanium disulfide, Transition metal carbyne complex, Transition metal indenyl complex, Transmetalation, Triisopropylamine, Trimethylsilyl cyanide, Trimethylsilyl iodide, Triphenylphosphine dichloride, Tris(benzyltriazolylmethyl)amine, Turbo-Hauser bases, Two-dimensional materials, Walden inversion, Wanzlick equilibrium, Zhao Yufen, Zhenan Bao, (R)-2-Methyl-CBS-oxazaborolidine, 1,2,4,5-Tetrabromobenzene, 1,4-Butane sultone, 1,8-Bis(dimethylamino)naphthalene, 1-Tetralone, 2,6-Xylenol, 2-Ethyl-2-oxazoline, 2-Phenylhexane. Expand index (150 more) »
Alan J. Heeger
Alan Jay Heeger (born January 22, 1936) is an American physicist, academic and Nobel Prize laureate in chemistry.
New!!: ChemComm and Alan J. Heeger · See more »
Aldol condensation
An aldol condensation is a condensation reaction in organic chemistry in which an enol or an enolate ion reacts with a carbonyl compound to form a β-hydroxyaldehyde or β-hydroxyketone (an aldol reaction), followed by dehydration to give a conjugated enone.
New!!: ChemComm and Aldol condensation · See more »
Aldol reaction
The aldol reaction is a means of forming carbon–carbon bonds in organic chemistry.
New!!: ChemComm and Aldol reaction · See more »
Alkyl nitrites
Alkyl nitrites are a group of chemical compounds based upon the molecular structure R-ONO.
New!!: ChemComm and Alkyl nitrites · See more »
Alkyne metathesis
Alkyne metathesis is an organic reaction involving the redistribution of alkyne chemical bonds.
New!!: ChemComm and Alkyne metathesis · See more »
Allylic rearrangement
An allylic rearrangement or allylic shift is an organic reaction in which the double bond in an allyl chemical compound shifts to the next carbon atom.
New!!: ChemComm and Allylic rearrangement · See more »
Andrew Bruce Holmes
Andrew Bruce Holmes,, (born 5 September 1943) is an Australian and British senior research chemist and professor at the Bio21 Institute, Melbourne, Australia, and the President of the Australian Academy of Science.
New!!: ChemComm and Andrew Bruce Holmes · See more »
Aromatization
Aromatization is a chemical reaction in which an aromatic system is formed.
New!!: ChemComm and Aromatization · See more »
Azide-alkyne Huisgen cycloaddition
The azide-alkyne Huisgen cycloaddition is a 1,3-dipolar cycloaddition between an azide and a terminal or internal alkyne to give a 1,2,3-triazole.
New!!: ChemComm and Azide-alkyne Huisgen cycloaddition · See more »
Baldwin's rules
Baldwin's rules in organic chemistry are a series of guidelines outlining the relative favorabilities of ring closure reactions in alicyclic compounds.
New!!: ChemComm and Baldwin's rules · See more »
Barton decarboxylation
The Barton decarboxylation is a radical reaction in which a carboxylic acid is first converted to a thiohydroxamate ester (commonly referred to as a Barton ester).
New!!: ChemComm and Barton decarboxylation · See more »
Barton–McCombie deoxygenation
The Barton–McCombie deoxygenation is an organic reaction in which an hydroxy functional group in an organic compound is replaced by a hydrogen to give an alkyl group.
New!!: ChemComm and Barton–McCombie deoxygenation · See more »
Beckmann rearrangement
The Beckmann rearrangement, named after the German chemist Ernst Otto Beckmann (1853–1923), is an acid-catalyzed rearrangement of an oxime to substituted amide.
New!!: ChemComm and Beckmann rearrangement · See more »
Ben Feringa
Bernard Lucas "Ben" Feringa (born 18 May 1951) is a Dutch synthetic organic chemist, specializing in molecular nanotechnology and homogenous catalysis.
New!!: ChemComm and Ben Feringa · See more »
Beta-peptide
β-peptides consist of β amino acids, which have their amino group bonded to the β carbon rather than the α carbon as in the 20 standard biological amino acids.
New!!: ChemComm and Beta-peptide · See more »
Biaxial nematic
A biaxial nematic is a spatially homogeneous liquid crystal with three distinct optical axes.
New!!: ChemComm and Biaxial nematic · See more »
Bis(cyclopentadienyl)titanium(III) chloride
Bis(cyclopentadienyl)titanium(III) chloride, also known as the Nugent–RajanBabu reagent, is the organotitanium compound which exists as a dimer with the formula 2.
New!!: ChemComm and Bis(cyclopentadienyl)titanium(III) chloride · See more »
Cambridge Structural Database
The Cambridge Structural Database (CSD) is both a repository and a validated and curated resource for the three-dimensional structural data of molecules generally containing at least carbon and hydrogen, comprising a wide range of organic, metal-organic and organometallic molecules.
New!!: ChemComm and Cambridge Structural Database · See more »
Carbene dye
A carbene dye is a reactive dye based on carbene chemistry.
New!!: ChemComm and Carbene dye · See more »
Carbon nanotube
Carbon nanotubes (CNTs) are allotropes of carbon with a cylindrical nanostructure.
New!!: ChemComm and Carbon nanotube · See more »
Carroll rearrangement
The Carroll rearrangement is a rearrangement reaction in organic chemistry and involves the transformation of a β-keto allyl ester into a α-allyl-β-ketocarboxylic acid.
New!!: ChemComm and Carroll rearrangement · See more »
CBS catalyst
The CBS catalyst or Corey–Bakshi–Shibata catalyst is an asymmetric catalyst derived from proline.
New!!: ChemComm and CBS catalyst · See more »
Chemical glycosylation
A chemical gycosylation reaction involves the coupling of a glycosyl donor, to a glycosyl acceptor forming a glycoside.
New!!: ChemComm and Chemical glycosylation · See more »
Chemical Science (journal)
Chemical Science is a monthly peer-reviewed scientific journal covering all aspects of chemistry.
New!!: ChemComm and Chemical Science (journal) · See more »
Cluster chemistry
In chemistry, a cluster is an ensemble of bound atoms or molecules that is intermediate in size between a molecule and a bulk solid.
New!!: ChemComm and Cluster chemistry · See more »
Cobalt(II) chloride
Cobalt(II) chloride is an inorganic compound of cobalt and chlorine, with the formula CoCl2.
New!!: ChemComm and Cobalt(II) chloride · See more »
Colin Raston
Colin Llewellyn Raston AO is a Professor of Chemistry of Flinders University in Adelaide, South Australia and the Premier's Professorial Fellow in Clean Technology.
New!!: ChemComm and Colin Raston · See more »
Copper(II) bromide
Copper(II) bromide (CuBr2) is a chemical compound.
New!!: ChemComm and Copper(II) bromide · See more »
Corey–Itsuno reduction
The Corey–Itsuno reduction, also known as the Corey–Bakshi–Shibata (CBS) reduction, is a chemical reaction in which an achiral ketone is enantioselectively reduced to produce the corresponding chiral, non-racemic alcohol.
New!!: ChemComm and Corey–Itsuno reduction · See more »
Crabtree's catalyst
Crabtree's catalyst is an organoiridium compound with the formula PF6.
New!!: ChemComm and Crabtree's catalyst · See more »
CrystEngComm
CrystEngComm is a peer-reviewed online-only scientific journal publishing original research and review articles on all aspects of crystal engineering including properties, polymorphism, target materials, and crystalline nanomaterials.
New!!: ChemComm and CrystEngComm · See more »
CrystEngCommunity
CrystEngCommunity is a virtual web community for people working in the field of crystal engineering.
New!!: ChemComm and CrystEngCommunity · See more »
Cucurbituril
Cucurbiturils are macrocyclic molecules made of glycoluril (.
New!!: ChemComm and Cucurbituril · See more »
David Klenerman
David Klenerman is a British biophysical chemist and a professor of biophysical chemistry at the Department of Chemistry at the University of Cambridge and a Fellow of Christ's College, Cambridge.
New!!: ChemComm and David Klenerman · See more »
Dendrimer
Dendrimers are repetitively branched molecules.
New!!: ChemComm and Dendrimer · See more »
Dewar benzene
Dewar benzene or bicyclohexa-2,5-diene is a bicyclic isomer of benzene with the molecular formula C6H6.
New!!: ChemComm and Dewar benzene · See more »
Di-tert-butyl dicarbonate
Di-tert-butyl dicarbonate is a reagent widely used in organic synthesis.
New!!: ChemComm and Di-tert-butyl dicarbonate · See more »
Di-tert-butyl peroxide
Di-tert-butyl peroxide or DTBP is an organic compound consisting of a peroxide group bonded to two tert-butyl groups.
New!!: ChemComm and Di-tert-butyl peroxide · See more »
Dianin's compound
Dianin's compound (4-p-hydroxyphenyl-2,2,4-trimethylchroman) was first prepared by Aleksandr Dianin in 1914.
New!!: ChemComm and Dianin's compound · See more »
Diarylethene
In chemistry, diarylethene is the general name of a class of compounds that have aromatic groups bonded to each end of a carbon–carbon double bond.
New!!: ChemComm and Diarylethene · See more »
Diborane(2)
Diborane(2) is an inorganic compound having the formula B2H2.
New!!: ChemComm and Diborane(2) · See more »
Dicarbonyltris(triphenylphosphine)ruthenium(0)
Dicarbonyltris(triphenylphosphine)ruthenium(0) or Roper's complex is a ruthenium metal carbonyl.
New!!: ChemComm and Dicarbonyltris(triphenylphosphine)ruthenium(0) · See more »
Dieter Seebach
Dieter Seebach is a German chemist known for his synthesis of biopolymers and dendrimers, and for his contributions to stereochemistry.
New!!: ChemComm and Dieter Seebach · See more »
Diethylamine
Diethylamine is an organic compound with the formula (CH3CH2)2NH.
New!!: ChemComm and Diethylamine · See more »
Dimethylcadmium
Dimethylcadmium is the organocadmium compound with the formula Cd(CH3)2.
New!!: ChemComm and Dimethylcadmium · See more »
Directed ortho metalation
Directed ortho metalation (DoM) is an adaptation of electrophilic aromatic substitution in which electrophiles attach themselves exclusively to the ortho- position of a direct metalation group or DMG through the intermediary of an aryllithium compound.
New!!: ChemComm and Directed ortho metalation · See more »
Don Tilley
T.
New!!: ChemComm and Don Tilley · See more »
Donald E. Pearson
Donald Emanuel Pearson "Doc", (June 21, 1914 in Madison, Wisconsin – April 14, 2004 in Nashville, Tennessee) was an American chemist and scientific researcher.
New!!: ChemComm and Donald E. Pearson · See more »
Douglas C. Gordon
Douglas Cameron Gordon, commonly known as Doug Gordon, (1956 – October 16, 1998) was an American whitewater kayaker, who was a member of the U.S. Slalom Team from 1981 to 1987, and a chemist.
New!!: ChemComm and Douglas C. Gordon · See more »
Electron affinity
In chemistry and atomic physics, the electron affinity (Eea) of an atom or molecule is defined as the amount of energy released or spent when an electron is added to a neutral atom or molecule in the gaseous state to form a negative ion.
New!!: ChemComm and Electron affinity · See more »
Enyne metathesis
An Enyne metathesis is an organic reaction taking place between an alkyne and an alkene with a metal carbene catalyst forming a butadiene.
New!!: ChemComm and Enyne metathesis · See more »
Ferrier carbocyclization
The Ferrier carbocyclization (or Ferrier II reaction) is an organic reaction that was first reported by the carbohydrate chemist Robert J. Ferrier in 1979.
New!!: ChemComm and Ferrier carbocyclization · See more »
Ferrocene
Ferrocene is an organometallic compound with the formula Fe(C5H5)2.
New!!: ChemComm and Ferrocene · See more »
Finkelstein reaction
The Finkelstein reaction (often referred to as a halex reaction or halogen exchange) named after the German chemist Hans Finkelstein, is an SN2 reaction (Substitution Nucleophilic Bimolecular reaction) that involves the exchange of one halogen atom for another.
New!!: ChemComm and Finkelstein reaction · See more »
Fleming–Tamao oxidation
The Fleming–Tamao oxidation, or Tamao–Kumada–Fleming oxidation, converts a carbon–silicon bond to a carbon–oxygen bond with a peroxy acid or hydrogen peroxide.
New!!: ChemComm and Fleming–Tamao oxidation · See more »
Fluoroantimonic acid
Fluoroantimonic acid is an inorganic compound with the chemical formula (also written, 2HF·SbF5, or simply HF-SbF5).
New!!: ChemComm and Fluoroantimonic acid · See more »
Four-center two-electron bond
A four-center two-electron bond (4c–2e bond) is a type of chemical bond in which four atoms share two electrons in bonding, with a net bond order of.
New!!: ChemComm and Four-center two-electron bond · See more »
Gautam Radhakrishna Desiraju
Gautam Radhakrishna Desiraju is an Indian chemist who has contributed substantially to the themes of crystal engineering and weak hydrogen bonding.
New!!: ChemComm and Gautam Radhakrishna Desiraju · See more »
Glutaconaldehyde
Glutaconaldehyde is an organic compound with the formula C5H6O2.
New!!: ChemComm and Glutaconaldehyde · See more »
Graphyne
Graphyne is a theorized allotrope of carbon.
New!!: ChemComm and Graphyne · See more »
Hajos–Parrish–Eder–Sauer–Wiechert reaction
The Hajos–Parrish–Eder–Sauer–Wiechert reaction in organic chemistry is a proline catalysed asymmetric aldol reaction.
New!!: ChemComm and Hajos–Parrish–Eder–Sauer–Wiechert reaction · See more »
Halogenation
Halogenation is a chemical reaction that involves the addition of one or more halogens to a compound or material.
New!!: ChemComm and Halogenation · See more »
Halonium ion
A halonium ion in organic chemistry is any onium compound (ion) containing a halogen atom carrying a positive charge.
New!!: ChemComm and Halonium ion · See more »
Hantzsch pyrrole synthesis
The Hantzsch Pyrrole Synthesis, named for Arthur Rudolf Hantzsch, is the chemical reaction of β-ketoesters (1) with ammonia (or primary amines) and α-haloketones (2) to give substituted pyrroles (3).
New!!: ChemComm and Hantzsch pyrrole synthesis · See more »
Hauser base
Hauser bases, also called magnesium amide bases, are magnesium compounds used in organic chemistry as bases for metalation reactions.
New!!: ChemComm and Hauser base · See more »
Hückel's rule
In organic chemistry, Hückel's rule estimates whether a planar ring molecule will have aromatic properties.
New!!: ChemComm and Hückel's rule · See more »
Heck reaction
The Heck reaction (also called the Mizoroki-Heck reaction) is the chemical reaction of an unsaturated halide (or triflate) with an alkene in the presence of a base and a palladium catalyst (or palladium nanomaterial-based catalyst) to form a substituted alkene.
New!!: ChemComm and Heck reaction · See more »
Henry Rzepa
Henry Stephen Rzepa (born 1950) is a chemist and Emeritus Professor of Computational chemistry at Imperial College London.
New!!: ChemComm and Henry Rzepa · See more »
Hexol
Hexol is the name for various salts of a coordination complex that has historical significance.
New!!: ChemComm and Hexol · See more »
High-temperature superconductivity
High-temperature superconductors (abbreviated high-Tc or HTS) are materials that behave as superconductors at unusually high temperatures.
New!!: ChemComm and High-temperature superconductivity · See more »
Hofmann–Löffler reaction
The Hofmann–Löffler reaction (also referred to as Hofmann–Löffler–Freytag reaction, Löffler–Freytag reaction, Löffler–Hofmann reaction, as well as Löffler's method) is an organic reaction in which a cyclic amine 2 (pyrrolidine or, in some cases, piperidine) is generated by thermal or photochemical decomposition of N-halogenated amine 1 in the presence of a strong acid (concentrated sulfuric acid or concentrated CF3CO2H).
New!!: ChemComm and Hofmann–Löffler reaction · See more »
Homochirality
Homochirality is a uniformity of chirality, or handedness.
New!!: ChemComm and Homochirality · See more »
Horner–Wadsworth–Emmons reaction
The Horner–Wadsworth–Emmons (HWE) reaction is a chemical reaction used in organic chemistry of stabilized phosphonate carbanions with aldehydes (or ketones) to produce predominantly E-alkenes.
New!!: ChemComm and Horner–Wadsworth–Emmons reaction · See more »
Hydrazine
Hydrazine is an inorganic compound with the chemical formula (also written), called diamidogen, archaically.
New!!: ChemComm and Hydrazine · See more »
Hydrazone iodination
Hydrazone iodination is an organic reaction in which a hydrazone is converted into a vinyl iodide by reaction of iodine and a non-nucleophilic base such as DBU.
New!!: ChemComm and Hydrazone iodination · See more »
Hydrocyanation
Hydrocyanation is, most fundamentally, the process whereby H+ and –CN ions are added to a molecular substrate.
New!!: ChemComm and Hydrocyanation · See more »
Hydroxylamine-O-sulfonic acid
Hydroxylamine-O-sulfonic acid ("HOSA") is the inorganic compound with molecular formula H3NO4S that is formed by the sulfonation of hydroxylamine with oleum.
New!!: ChemComm and Hydroxylamine-O-sulfonic acid · See more »
Intramolecular reaction
Intramolecular in chemistry describes a process or characteristic limited within the structure of a single molecule, a property or phenomenon limited to the extent of a single molecule.
New!!: ChemComm and Intramolecular reaction · See more »
Iodane
Iodanes are chemical compounds containing hypervalent iodine.
New!!: ChemComm and Iodane · See more »
Iodosobenzene
Iodosobenzene or iodosylbenzene is an organoiodine compound with the empirical formula C6H5IO.
New!!: ChemComm and Iodosobenzene · See more »
Ionic liquid
An ionic liquid (IL) is a salt in the liquid state.
New!!: ChemComm and Ionic liquid · See more »
Irshad Hussain
Irshad Hussain (ارشاد حسین) is a Pakistani Chemist and among the few pioneers to initiate nanomaterials research in Pakistan.
New!!: ChemComm and Irshad Hussain · See more »
Isomer
An isomer (from Greek ἰσομερής, isomerès; isos.
New!!: ChemComm and Isomer · See more »
Isomerization
In chemistry isomerization (also isomerisation) is the process by which one molecule is transformed into another molecule which has exactly the same atoms, but the atoms have a different arrangement e.g. A-B-C → B-A-C (these related molecules are known as isomers). In some molecules and under some conditions, isomerization occurs spontaneously.
New!!: ChemComm and Isomerization · See more »
Johnson–Corey–Chaykovsky reaction
The Johnson–Corey–Chaykovsky reaction (sometimes referred to as the Corey–Chaykovsky reaction or CCR) is a chemical reaction used in organic chemistry for the synthesis of epoxides, aziridines, and cyclopropanes.
New!!: ChemComm and Johnson–Corey–Chaykovsky reaction · See more »
Journal of the Chemical Society
The Journal of the Chemical Society was a scientific journal established by the Chemical Society in 1849 as the Quarterly Journal of the Chemical Society.
New!!: ChemComm and Journal of the Chemical Society · See more »
Juliá–Colonna epoxidation
The Juliá–Colonna epoxidation is an asymmetric poly-leucine catalyzed nucleophilic epoxidation of electron deficient olefins in a triphasic system.
New!!: ChemComm and Juliá–Colonna epoxidation · See more »
Krogmann's salt
Krogmann's salt is a mixed-valence square planar coordination complex of platinum and cyanide bonded through linear platinum metal chains, sometimes described as molecular wires.
New!!: ChemComm and Krogmann's salt · See more »
Lanthanide trifluoromethanesulfonates
Lanthanide triflates are triflate salts of the lanthanide family with many uses in organic chemistry as Lewis acid catalysts.
New!!: ChemComm 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!!: ChemComm and Lawesson's reagent · See more »
Lead
Lead is a chemical element with symbol Pb (from the Latin plumbum) and atomic number 82.
New!!: ChemComm and Lead · See more »
Lead(II) nitrate
Lead(II) nitrate is an inorganic compound with the chemical formula Pb(NO3)2.
New!!: ChemComm and Lead(II) nitrate · See more »
List of chemistry journals
This is a list of scientific journals in chemistry and its various subfields.
New!!: ChemComm and List of chemistry journals · See more »
List of Royal Society of Chemistry journals
This is a list of scientific journals published by the Royal Society of Chemistry.
New!!: ChemComm and List of Royal Society of Chemistry journals · See more »
List of scientific journals
The following is a partial list of scientific journals.
New!!: ChemComm and List of scientific journals · See more »
Lithium nitride
Lithium nitride is a compound with the formula Li3N.
New!!: ChemComm and Lithium nitride · See more »
Luche reduction
Luche reduction is the selective organic reduction of α,β-unsaturated ketones to allylic alcohols with sodium borohydride (NaBH4) and lanthanide chlorides, mainly cerium(III) chloride (CeCl3), in methanol or ethanol.
New!!: ChemComm and Luche reduction · See more »
Markó–Lam deoxygenation
The Markó–Lam deoxygenation is an organic chemistry reaction where the hydroxy functional group in an organic compound is replaced by a hydrogen atom to give an alkyl group.
New!!: ChemComm and Markó–Lam deoxygenation · See more »
Martin A. Bennett
Martin Arthur Bennett FRS is an Australian inorganic chemist.
New!!: ChemComm and Martin A. Bennett · See more »
Mauveine
Mauveine, also known as aniline purple and Perkin's mauve, was the first synthetic dye.
New!!: ChemComm and Mauveine · See more »
Mechanically interlocked molecular architectures
Mechanically interlocked molecular architectures (MIMAs) are molecules that are connected as a consequence of their topology.
New!!: ChemComm and Mechanically interlocked molecular architectures · See more »
Metal acetylacetonates
Metal acetylacetonates are coordination complexes derived from the acetylacetonate anion and metal ions, usually transition metals.
New!!: ChemComm and Metal acetylacetonates · See more »
Metal aromaticity
Metal aromaticity is the concept of aromaticity found in many organic compounds is extended to metals.
New!!: ChemComm and Metal aromaticity · See more »
Metal–organic framework
Metal–organic frameworks (MOFs) are compounds consisting of metal ions or clusters coordinated to organic ligands to form one-, two-, or three-dimensional structures.
New!!: ChemComm and Metal–organic framework · See more »
Metallabenzene
The parent metallacyclobenzene has the formula LnM(CH)5.
New!!: ChemComm and Metallabenzene · See more »
Microreactor
A microreactor or microstructured reactor or microchannel reactor is a device in which chemical reactions take place in a confinement with typical lateral dimensions below 1 mm; the most typical form of such confinement are microchannels.
New!!: ChemComm and Microreactor · See more »
Molecular Borromean rings
Molecular Borromean rings are an example of a mechanically-interlocked molecular architecture in which three macrocycles are interlocked in such a way that breaking any macrocycle allows the others to disassociate.
New!!: ChemComm and Molecular Borromean rings · See more »
Murchison meteorite
The Murchison meteorite is a large meteorite that fell to earth near Murchison, Victoria, in Australia, in 1969.
New!!: ChemComm and Murchison meteorite · See more »
N-Chlorosuccinimide
N-Chlorosuccinimide is used for chlorinations and as a mild oxidant.
New!!: ChemComm and N-Chlorosuccinimide · See more »
Nanofiber seeding
Nanofiber Seeding is a process to control the bulk morphology of chemically synthesized conducting polymers.
New!!: ChemComm and Nanofiber seeding · See more »
Nazarov cyclization reaction
The Nazarov cyclization reaction (often referred to as simply the Nazarov cyclization) is a chemical reaction used in organic chemistry for the synthesis of cyclopentenones.
New!!: ChemComm and Nazarov cyclization reaction · See more »
Nitrile
A nitrile is any organic compound that has a −C≡N functional group.
New!!: ChemComm and Nitrile · See more »
Nitrilimine
Nitrilimines or nitrile amides are a class of organic compounds sharing a common functional group with the general structure R-CN-NR corresponding to the conjugate base of an amine bonded to the N-terminus of a nitrile.
New!!: ChemComm and Nitrilimine · See more »
Nitrogen
Nitrogen is a chemical element with symbol N and atomic number 7.
New!!: ChemComm and Nitrogen · See more »
Nitrone-olefin (3+2) cycloaddition
The nitrone-olefin (3+2) cycloaddition reaction is the combination of a nitrone with an alkene or alkyne to generate an isoxazoline or isoxazolidine via a cycloaddition process.
New!!: ChemComm and Nitrone-olefin (3+2) cycloaddition · See more »
Noble gas compound
Noble gas compounds are chemical compounds that include an element from the noble gases, group 18 of the periodic table.
New!!: ChemComm and Noble gas compound · 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!!: ChemComm and On water reaction · See more »
Organic and Biomolecular Chemistry
Organic & Biomolecular Chemistry is a biweekly peer-reviewed scientific journal covering all aspects of organic chemistry, including organic aspects of chemical biology, medicinal chemistry, natural product chemistry, supramolecular chemistry, macromolecular chemistry, theoretical chemistry, and catalysis.
New!!: ChemComm and Organic and Biomolecular Chemistry · See more »
Organocadmium compound
An organocadmium compound is an organometallic compound containing a carbon to cadmium chemical bond.
New!!: ChemComm and Organocadmium compound · See more »
Organonickel
Organonickel chemistry is a branch of organometallic chemistry that deals with organic compounds featuring nickel-carbon bonds.
New!!: ChemComm and Organonickel · See more »
Organopalladium
Organopalladium chemistry is a branch of organometallic chemistry that deals with organic palladium compounds and their reactions.
New!!: ChemComm and Organopalladium · See more »
Organophosphorus compound
Organophosphorus compounds are organic compounds containing phosphorus.
New!!: ChemComm and Organophosphorus compound · See more »
Organosilicon
Organosilicon compounds are organometallic compounds containing carbon–silicon bonds.
New!!: ChemComm and Organosilicon · See more »
Organotellurium chemistry
Organotellurium chemistry in chemistry describes the synthesis and properties of chemical compounds containing a carbon to tellurium chemical bond.
New!!: ChemComm and Organotellurium chemistry · See more »
Osmium(IV) chloride
Osmium(IV) chloride or osmium tetrachloride is the inorganic compound composed of osmium and chlorine with the empirical formula OsCl4.
New!!: ChemComm and Osmium(IV) chloride · See more »
Oxazole
Oxazole is the parent compound for a vast class of heterocyclic aromatic organic compounds.
New!!: ChemComm and Oxazole · See more »
P4-t-Bu
P4-t-Bu is a readily accessible chemical from the group of neutral, peralkylated sterically hindered polyaminophosphazenes, which are extremely strong bases but very weak nucleophiles.
New!!: ChemComm and P4-t-Bu · See more »
Paal–Knorr synthesis
The Paal–Knorr Synthesis in organic chemistry is a reaction that generates either furans, pyrroles, or thiophenes from 1,4-diketones.
New!!: ChemComm and Paal–Knorr synthesis · See more »
Paclitaxel total synthesis
Paclitaxel total synthesis in organic chemistry is a major ongoing research effort in the total synthesis of paclitaxel (Taxol).
New!!: ChemComm and Paclitaxel total synthesis · See more »
Paolo Samorì
Paolo Samorì (born in Imola, Italy, 1971) is an Italian physical chemist and Distinguished Professor (PRCE) and director of the Institut de Science et d'Ingénierie Supramoléculaires (ISIS) of the Université de Strasbourg (UdS) where he is also head of the Nanochemistry Laboratory.
New!!: ChemComm and Paolo Samorì · See more »
Paramasivam Natarajan
Paramasivam Natarajan (1940–2016) was an Indian photochemist, the INSA Senior Scientist at the National Centre for Ultrafast Process of the University of Madras and the Director of Central Salt and Marine Chemicals Research Institute (CSMCRI) of the Council of Scientific and Industrial Research.
New!!: ChemComm and Paramasivam Natarajan · See more »
Pentacene
Pentacene is a polycyclic aromatic hydrocarbon consisting of five linearly-fused benzene rings.
New!!: ChemComm and Pentacene · See more »
Pentamethylcyclopentadiene
1,2,3,4,5-Pentamethylcyclopentadiene is a cyclic dialkene with the formula C5Me5H (Me.
New!!: ChemComm and Pentamethylcyclopentadiene · See more »
Pentamethylcyclopentadienyl rhodium dichloride dimer
Pentamethylcyclopentadienyl rhodium dichloride is an organometallic compound with the formula 2, commonly abbreviated 2 This dark red air-stable diamagnetic solid is a reagent in organometallic chemistry.
New!!: ChemComm and Pentamethylcyclopentadienyl rhodium dichloride dimer · See more »
Peptide synthesis
In organic chemistry, peptide synthesis is the production of peptides, compounds where multiple amino acids are linked via amide bonds, also known as peptide bonds.
New!!: ChemComm and Peptide synthesis · See more »
Persistent carbene
A persistent carbene (also known as stable carbene) is a type of carbene demonstrating particular stability.
New!!: ChemComm and Persistent carbene · See more »
Peter Maitlis
Peter Michael Maitlis, FRS (born 15 January 1933) is a retired British organometallic chemist.
New!!: ChemComm and Peter Maitlis · See more »
Phase-boundary catalysis
In chemistry, phase-boundary catalysis (PBC) is a type of heterogeneous catalytic system which facilitates the chemical reaction of a particular chemical component in an immiscible phase to react on a catalytic active site located at a phase boundary.
New!!: ChemComm and Phase-boundary catalysis · See more »
Phenylacetylene
Phenylacetylene is an alkyne hydrocarbon containing a phenyl group.
New!!: ChemComm and Phenylacetylene · See more »
Phenylboronic acid
Phenylboronic acid or benzeneboronic acid, abbreviated as PhB(OH)2 where Ph is the phenyl group C6H5-, is a boronic acid containing a phenyl substituent and two hydroxyl groups attached to boron.
New!!: ChemComm and Phenylboronic acid · See more »
Phosphonium
The phosphonium (more obscurely: phosphinium) cation describes polyatomic cations with the chemical formula.
New!!: ChemComm and Phosphonium · See more »
Phosphorus triiodide
Phosphorus triiodide (PI3) is an unstable red solid which reacts violently with water.
New!!: ChemComm and Phosphorus triiodide · See more »
Pi bond
In chemistry, pi bonds (π bonds) are covalent chemical bonds where two lobes of an orbital on one atom overlap two lobes of an orbital on another atom.
New!!: ChemComm and Pi bond · See more »
PMDTA
PMDTA (N,N,N′,N′′,N′′-pentamethyldiethylenetriamine) is an organic compound with the formula 2NCH3.
New!!: ChemComm and PMDTA · See more »
Polymorphism (materials science)
In materials science, polymorphism is the ability of a solid material to exist in more than one form or crystal structure.
New!!: ChemComm and Polymorphism (materials science) · See more »
Pummerer rearrangement
The Pummerer rearrangement is an organic reaction whereby an alkyl sulfoxide rearranges to an α-acyloxy–thioether in the presence of acetic anhydride.
New!!: ChemComm and Pummerer rearrangement · See more »
Pyrylium salt
The pyrylium cation is a six-membered, unsaturated, mono-cyclic compound.
New!!: ChemComm and Pyrylium salt · See more »
Quintuple bond
A quintuple bond in chemistry is an unusual type of chemical bond, first reported in 2005 for a dichromium compound.
New!!: ChemComm and Quintuple bond · See more »
Radon
Radon is a chemical element with symbol Rn and atomic number 86.
New!!: ChemComm and Radon · See more »
Radon difluoride
Radon difluoride is a compound of radon, a noble gas.
New!!: ChemComm and Radon difluoride · See more »
Ramberg–Bäcklund reaction
The Ramberg–Bäcklund reaction is an organic reaction converting an α-halo sulfone into an alkene in presence of a base with extrusion of sulfur dioxide.
New!!: ChemComm and Ramberg–Bäcklund reaction · See more »
Resorcinarene
A resorcinarene (also resorcarene or calixresorcinarene) is a macrocycle, or a cyclic oligomer, based on the condensation of resorcinol (1,3-dihydroxybenzene) and an aldehyde.
New!!: ChemComm and Resorcinarene · See more »
Roger Alder
Roger William Alder, FRS is an Emeritus Professor of organic chemistry at the University of Bristol.
New!!: ChemComm and Roger Alder · See more »
Rotaxane
A rotaxane is a mechanically interlocked molecular architecture consisting of a "dumbbell shaped molecule" which is threaded through a "macrocycle" (see graphical representation).
New!!: ChemComm and Rotaxane · See more »
Royal Society of Chemistry
The Royal Society of Chemistry (RSC) is a learned society (professional association) in the United Kingdom with the goal of "advancing the chemical sciences".
New!!: ChemComm and Royal Society of Chemistry · See more »
RSC Advances
RSC Advances is an online-only peer-reviewed scientific journal covering research on all aspects of the chemical sciences.
New!!: ChemComm and RSC Advances · See more »
Saegusa–Ito oxidation
The Saegusa–Ito oxidation is a chemical reaction used in organic chemistry.
New!!: ChemComm and Saegusa–Ito oxidation · See more »
Salt bridge (protein and supramolecular)
In chemistry, a salt bridge is a combination of two non-covalent interactions: hydrogen bonding and ionic bonding (Figure 1).
New!!: ChemComm and Salt bridge (protein and supramolecular) · See more »
Sandeep Verma
Sandeep Verma (born 1966) is an Indian bioorganic chemist and a professor of the department of chemistry at the Indian Institute of Technology, Kanpur (IITK).
New!!: ChemComm and Sandeep Verma · See more »
Sandwich compound
In organometallic chemistry, a sandwich compound is a chemical compound featuring a metal bound by haptic covalent bonds to two arene ligands.
New!!: ChemComm and Sandwich compound · See more »
Schwartz's reagent
Schwartz's reagent is the common name for the chemical compound with the formula (C5H5)2ZrHCl, sometimes called zirconocene hydrochloride or zirconocene chloride hydride, and is named after Jeffrey Schwartz, a chemistry professor at Princeton University.
New!!: ChemComm and Schwartz's reagent · See more »
Sigmatropic reaction
A sigmatropic reaction in organic chemistry is a pericyclic reaction wherein the net result is one σ-bond is changed to another σ-bond in an uncatalyzed intramolecular process.
New!!: ChemComm and Sigmatropic reaction · See more »
Silver acetylide
Silver acetylide is an inorganic chemical compound with the formula Ag2C2, a metal acetylide.
New!!: ChemComm and Silver acetylide · See more »
Single-molecule magnet
Single-molecule magnets (SMM) are a class of metalorganic compounds that show superparamagnetic behavior below a certain blocking temperature at the molecular scale.
New!!: ChemComm and Single-molecule magnet · See more »
Solubility
Solubility is the property of a solid, liquid or gaseous chemical substance called solute to dissolve in a solid, liquid or gaseous solvent.
New!!: ChemComm and Solubility · See more »
Sonogashira coupling
The Sonogashira reaction is a cross-coupling reaction used in organic synthesis to form carbon–carbon bonds.
New!!: ChemComm and Sonogashira coupling · See more »
Sumanene
Sumanene is a polycyclic aromatic hydrocarbon and of scientific interest because the molecule can be considered a fragment of buckminsterfullerene.
New!!: ChemComm and Sumanene · See more »
Supercritical fluid
A supercritical fluid (SCF) is any substance at a temperature and pressure above its critical point, where distinct liquid and gas phases do not exist.
New!!: ChemComm and Supercritical fluid · 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!!: ChemComm and Supramolecular catalysis · See more »
Supramolecular electronics
Supramolecular electronics is the experimental field of supramolecular chemistry that bridges the gap between molecular electronics and bulk plastics in the construction of electronic circuitry at the nanoscale 1.
New!!: ChemComm and Supramolecular electronics · See more »
Synthetic setae
Synthetic setae emulate the setae found on the toes of a gecko and scientific research in this area is driven towards the development of dry adhesives.
New!!: ChemComm and Synthetic setae · See more »
Taxodone
Taxodone is a naturally occurring diterpenoid found in Taxodium distichum (Bald Cypress), Rosmarinus officinalis (Rosemary), several Salvia species and other plants, along with its oxidized rearrangement product, taxodione.
New!!: ChemComm and Taxodone · See more »
Tert-Butyloxycarbonyl protecting group
The tert-butyloxycarbonyl protecting group (BOC group) is a protecting group used in organic synthesis.
New!!: ChemComm and Tert-Butyloxycarbonyl protecting group · See more »
Tetramethylurea
Tetramethylurea is a aprotic-polar solvent for organic compounds, especially for aromatic compounds and is used e. g. for Grignard reagents.
New!!: ChemComm and Tetramethylurea · See more »
Tetrapropylammonium perruthenate
Tetrapropylammonium perruthenate (TPAP or TPAPR) is the chemical compound described by the formula N(C3H7)4RuO4.
New!!: ChemComm and Tetrapropylammonium perruthenate · 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!!: ChemComm and Thiazole · See more »
Thin-layer chromatography
Thin-layer chromatography (TLC) is a chromatography technique used to separate non-volatile mixtures.
New!!: ChemComm and Thin-layer chromatography · See more »
Titanium disulfide
Titanium disulfide is an inorganic compound with the formula TiS2.
New!!: ChemComm and Titanium disulfide · See more »
Transition metal carbyne complex
Transition metal carbyne complexes are organometallic compounds with a triple bond between carbon and the transition metal.
New!!: ChemComm and Transition metal carbyne complex · See more »
Transition metal indenyl complex
In organometallic chemistry, a transition metal indenyl complex is a coordination compound that contains one or more indenyl ligands.
New!!: ChemComm and Transition metal indenyl complex · See more »
Transmetalation
Transmetalation (alt. spelling: transmetallation) is a type of organometallic reaction that involves the transfer of ligands from one metal to another.
New!!: ChemComm and Transmetalation · See more »
Triisopropylamine
Triisopropylamine is an organic chemical compound consisting of three isopropyl groups bound to a central nitrogen atom.
New!!: ChemComm and Triisopropylamine · See more »
Trimethylsilyl cyanide
Trimethylsilyl cyanide is the chemical compound with the formula (CH3)3SiCN.
New!!: ChemComm and Trimethylsilyl cyanide · See more »
Trimethylsilyl iodide
Trimethylsilyl iodide (iodotrimethylsilane or TMSI) is an organosilicon compound with the chemical formula (CH3)3SiI.
New!!: ChemComm and Trimethylsilyl iodide · See more »
Triphenylphosphine dichloride
Triphenylphosphine dichloride, Ph3PCl2, is a chlorinating agent widely used in organic chemistry.
New!!: ChemComm and Triphenylphosphine dichloride · See more »
Tris(benzyltriazolylmethyl)amine
Tris((1-benzyl-4-triazolyl)methyl)amine (TBTA) is a tertiary amine containing the 1,2,3-triazole moiety.
New!!: ChemComm and Tris(benzyltriazolylmethyl)amine · See more »
Turbo-Hauser bases
Turbo-Hauser bases are amido magnesium halides that contain stoichiometric amounts of LiCl.
New!!: ChemComm and Turbo-Hauser bases · See more »
Two-dimensional materials
2D Materials, sometimes referred to as single layer materials, are crystalline materials consisting of a single layer of atoms.
New!!: ChemComm and Two-dimensional materials · See more »
Walden inversion
Walden inversion is the inversion of a chiral center in a molecule in a chemical reaction.
New!!: ChemComm and Walden inversion · See more »
Wanzlick equilibrium
The Wanzlick equilibrium is a chemical equilibrium between a relatively stable carbene compound and its dimer.
New!!: ChemComm and Wanzlick equilibrium · See more »
Zhao Yufen
Zhao Yufen (born 1948) is a chemist and researcher at the College of Chemistry and Chemical Engineering at Xiamen University.
New!!: ChemComm and Zhao Yufen · See more »
Zhenan Bao
Zhenan Bao (born 1970), Ph.D., is a Professor of Chemical Engineering and Material Science and Engineering at Stanford University.
New!!: ChemComm and Zhenan Bao · See more »
(R)-2-Methyl-CBS-oxazaborolidine
(R)-2-Methyl-CBS-oxazaborolidine is an organoboron catalyst that is used in organic synthesis.
New!!: ChemComm and (R)-2-Methyl-CBS-oxazaborolidine · 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!!: ChemComm and 1,2,4,5-Tetrabromobenzene · See more »
1,4-Butane sultone
1,4-butane sultone is a six-membered δ-sultone and the cyclic ester of 4-hydroxybutanesulfonic acid.
New!!: ChemComm and 1,4-Butane sultone · See more »
1,8-Bis(dimethylamino)naphthalene
1,8-Bis(dimethylamino)naphthalene is an organic compound with the formula C10H6(NMe2)2 (Me.
New!!: ChemComm and 1,8-Bis(dimethylamino)naphthalene · See more »
1-Tetralone
1-Tetralone is a bicyclic aromatic hydrocarbon with an α-keto group (a benzocycloalkanone) and can also be regarded as benzo-fused cyclohexanone.
New!!: ChemComm and 1-Tetralone · See more »
2,6-Xylenol
2,6-Xylenol is a chemical compound which is one of the six isomers of xylenol.
New!!: ChemComm and 2,6-Xylenol · See more »
2-Ethyl-2-oxazoline
2-Ethyl-2-oxazoline (EtOx) is an oxazoline which is used particularly as a monomer for the cationic ring-opening polymerization to poly(2-alkyloxazoline)s.
New!!: ChemComm and 2-Ethyl-2-oxazoline · See more »
2-Phenylhexane
2-Phenylhexane is an aromatic hydrocarbon.
New!!: ChemComm and 2-Phenylhexane · See more »
Redirects here:
Chem Commun, Chem Commun (Camb), Chem. Comm., Chem. Commun., Chem. Commun. (Camb.), Chem. Commun. (London), Chemical Communications, J Chem Soc Chem Commun, J. Chem Soc., Chem. Commun., J. Chem. Soc. Chem. Commun., J. Chem. Soc., Chem. Commun., Journal of the Chemical Society, Chemical Communications.
References
[1] https://en.wikipedia.org/wiki/ChemComm