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70 relations: Acyloin, Alcohol, Amination, Ammonia, Butanone, Carbonyl group, Chelation, Chemical Abstracts Service, Chemical Reviews, Chemical Society Reviews, Chemische Berichte, Chemistry: A European Journal, Chiral auxiliary, Chirality (chemistry), Cis–trans isomerism, Cumulene, Cycloaddition, Dioxirane, Electronegativity, Electrophile, Enantiomeric excess, Enantioselective synthesis, Enol, Enone, Epoxide, Erectile dysfunction, Franklin A. Davis, Giuseppe Resnati, Heterocyclic compound, Holton Taxol total synthesis, Hydrazine, Hydrogen peroxide, Imine, Jacobsen epoxidation, Journal of Organic Chemistry, Journal of the American Chemical Society, Juliá–Colonna epoxidation, Lactam, Meta-Chloroperoxybenzoic acid, MoOPH, National Institutes of Health, Nitrone, Nucleophile, Okadaic acid, Organic compound, Organic Letters, Organic Syntheses, Perfluorinated compound, Peroxide process, Peroxy acid, ..., Phase-transfer catalyst, Potassium peroxymonosulfate, Radical (chemistry), Selective serotonin reuptake inhibitor, Selenide, Sharpless epoxidation, Spiro compound, Stereoelectronic effect, Stereospecificity, Steric effects, Sulfide, Tertiary carbon, Tetrahedron (journal), Tetrahedron Letters, Thermodynamics, Thioether, Thiol, Wender Taxol total synthesis, William D. Emmons, Yohimbine. Expand index (20 more) »
Acyloin
Acyloins or α-hydroxy ketones are a class of organic compounds which all possess a hydroxy group adjacent to a ketone group.
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Alcohol
In chemistry, an alcohol is any organic compound in which the hydroxyl functional group (–OH) is bound to a carbon.
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Amination
Amination is the process by which an amine group is introduced into an organic molecule.
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Ammonia
Ammonia is a compound of nitrogen and hydrogen with the formula NH3.
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Butanone
Butanone, also known as methyl ethyl ketone (MEK), is an organic compound with the formula CH3C(O)CH2CH3.
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Carbonyl group
In organic chemistry, a carbonyl group is a functional group composed of a carbon atom double-bonded to an oxygen atom: C.
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Chelation
Chelation is a type of bonding of ions and molecules to metal ions.
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Chemical Abstracts Service
Chemical Abstracts Service (CAS) is a division of the American Chemical Society.
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Chemical Reviews
Chemical Reviews is peer-reviewed scientific journal published twice per month by the American Chemical Society.
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Chemical Society Reviews
Chemical Society Reviews is a biweekly peer-reviewed scientific journal published by the Royal Society of Chemistry, for review articles on topics of current interest in chemistry.
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Chemische Berichte
Chemische Berichte (usually abbreviated as Ber. or Chem. Ber.) was a German-language scientific journal of all disciplines of chemistry founded in 1868.
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Chemistry: A European Journal
Chemistry: A European Journal is a peer-reviewed scientific journal that publishes articles on all areas of chemistry and related fields.
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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.
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Chirality (chemistry)
Chirality is a geometric property of some molecules and ions.
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Cis–trans isomerism
Cis–trans isomerism, also known as geometric isomerism or configurational isomerism, is a term used in organic chemistry.
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Cumulene
A cumulene is a hydrocarbon with three or more cumulative (consecutive) double bonds.
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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.
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Dioxirane
In chemistry dioxirane is a heterocyclic compound composed of one carbon and two oxygen atoms; it may be thought of as the smallest cyclic organic peroxide.
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Electronegativity
Electronegativity, symbol ''χ'', is a chemical property that describes the tendency of an atom to attract a shared pair of electrons (or electron density) towards itself.
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Electrophile
In organic chemistry, an electrophile is a reagent attracted to electrons.
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Enantiomeric excess
Enantiomeric excess (ee) is a measurement of purity used for chiral substances.
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Enantioselective synthesis
Enantioselective synthesis, also called asymmetric synthesis, is a form of chemical synthesis.
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Enol
Enols, or more formally, alkenols, are a type of reactive structure or intermediate in organic chemistry that is represented as an alkene (olefin) with a hydroxyl group attached to one end of the alkene double bond.
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Enone
An enone, also called an α,β-unsaturated carbonyl, is a type of organic compound consisting of an alkene conjugated to a ketone.
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Epoxide
An epoxide is a cyclic ether with a three-atom ring.
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Erectile dysfunction
Erectile dysfunction (ED), also known as impotence, is a type of sexual dysfunction characterized by the inability to develop or maintain an erection of the penis during sexual activity.
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Franklin A. Davis
Franklin Arnold Davis (born April 1, 1939) is the Laura H. Carnell Professor of Chemistry at Temple University in Philadelphia, Pennsylvania.
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Giuseppe Resnati
Giuseppe Resnati (born 26 August 1955) is an Italian chemist with interests in fluorine chemistry and supramolecular chemistry.
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Heterocyclic compound
A heterocyclic compound or ring structure is a cyclic compound that has atoms of at least two different elements as members of its ring(s).
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Holton Taxol total synthesis
The Holton Taxol total synthesis, published by Robert A. Holton and his group at Florida State University in 1994 was the first total synthesis of Taxol (generic name: paclitaxel).
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Hydrazine
Hydrazine is an inorganic compound with the chemical formula (also written), called diamidogen, archaically.
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Hydrogen peroxide
Hydrogen peroxide is a chemical compound with the formula.
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Imine
An imine is a functional group or chemical compound containing a carbon–nitrogen double bond.
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Jacobsen epoxidation
The Jacobsen epoxidation, sometimes also referred to as Jacobsen-Katsuki epoxidation is a chemical reaction which allows enantioselective epoxidation of unfunctionalized alkyl- and aryl- substituted olefins.
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Journal of Organic Chemistry
The Journal of Organic Chemistry, colloquially known as JOC or J Org, is a peer-reviewed scientific journal for original contributions of fundamental research in all branches of theory and practice in organic and bioorganic chemistry.
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Journal of the American Chemical Society
The Journal of the American Chemical Society (also known as JACS) is a weekly peer-reviewed scientific journal that was established in 1879 by the American Chemical Society.
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Juliá–Colonna epoxidation
The Juliá–Colonna epoxidation is an asymmetric poly-leucine catalyzed nucleophilic epoxidation of electron deficient olefins in a triphasic system.
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Lactam
A lactam is a cyclic amide.
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Meta-Chloroperoxybenzoic acid
meta-Chloroperoxybenzoic acid (mCPBA) is a peroxycarboxylic acid used widely as an oxidant in organic synthesis.
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MoOPH
MoOPH, also known as oxodiperoxymolybdenum(pyridine)-(hexamethylphosphoric triamide), is a reagent used in organic synthesis.
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National Institutes of Health
The National Institutes of Health (NIH) is the primary agency of the United States government responsible for biomedical and public health research, founded in the late 1870s.
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Nitrone
A nitrone is a functional group in organic chemistry consisting of an ''N''-oxide of an imine.
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Nucleophile
Nucleophile is a chemical species that donates an electron pair to an electrophile to form a chemical bond in relation to a reaction.
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Okadaic acid
Okadaic acid, C44H68O13, is a toxin produced by several species of dinoflagellates, and is known to accumulate in both marine sponges and shellfish.
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Organic compound
In chemistry, an organic compound is generally any chemical compound that contains carbon.
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Organic Letters
Organic Letters (usually abbreviated as Org. Lett.), is a peer-reviewed biweekly scientific journal, published since 1999 by the American Chemical Society.
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Organic Syntheses
Organic Syntheses is a peer-reviewed scientific journal that was established in 1921.
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Perfluorinated compound
A perfluorinated compound (PFC) per- or polyfluoroalkyl chemical is an organofluorine compound containing only carbon-fluorine bonds (no C-H bonds) and C-C bonds but also other heteroatoms.
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Peroxide process
The peroxide process is a method for the industrial production of hydrazine.
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Peroxy acid
A peroxy acid (often spelled as one word, peroxyacid, and sometimes called peracid) is an acid which contains an acidic –OOH group.
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Phase-transfer catalyst
In chemistry, a phase-transfer catalyst or PTC is a catalyst that facilitates the migration of a reactant from one phase into another phase where reaction occurs.
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Potassium peroxymonosulfate
Potassium peroxymonosulfate (also known as MPS, potassium monopersulfate, potassium caroate, and the trade names Caroat and Oxone) is widely used as an oxidizing agent.
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Radical (chemistry)
In chemistry, a radical (more precisely, a free radical) is an atom, molecule, or ion that has an unpaired valence electron.
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Selective serotonin reuptake inhibitor
Selective serotonin reuptake inhibitors (SSRIs) are a class of drugs that are typically used as antidepressants in the treatment of major depressive disorder and anxiety disorders.
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Selenide
A selenide is a chemical compound containing a selenium anion with oxidation number of −2 (Se2&minus), much as sulfur does in a sulfide.
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Sharpless epoxidation
The Sharpless epoxidation reaction is an enantioselective chemical reaction to prepare 2,3-epoxyalcohols from primary and secondary allylic alcohols.
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Spiro compound
A spiro compound, or spirane, from the Latin spīra, meaning a twist or coil, For a further but less stable source of the same text that provides access to the relevant material, see, same access date.
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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.
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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.
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Steric effects
Steric effects are nonbonding interactions that influence the shape (conformation) and reactivity of ions and molecules.
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Sulfide
Sulfide (systematically named sulfanediide, and sulfide(2−)) (British English sulphide) is an inorganic anion of sulfur with the chemical formula S2− or a compound containing one or more S2− ions.
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Tertiary carbon
A tertiary carbon atom is a carbon atom bound to three other carbon atoms.
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Tetrahedron (journal)
Tetrahedron is a weekly peer-reviewed scientific journal covering the field of organic chemistry.
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Tetrahedron Letters
Tetrahedron Letters is a weekly international journal for rapid publication of full original research papers in the field of organic chemistry.
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Thermodynamics
Thermodynamics is the branch of physics concerned with heat and temperature and their relation to energy and work.
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Thioether
A thioether is a functional group in organosulfur chemistry with the connectivity C–S–C as shown on right.
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Thiol
Thiol is an organosulfur compound that contains a carbon-bonded sulfhydryl (R–SH) group (where R represents an alkyl or other organic substituent).
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Wender Taxol total synthesis
The Wender Taxol total synthesis in organic chemistry describes a Taxol total synthesis (one of six to date) by the group of Paul Wender at Stanford University published in 1997.
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William D. Emmons
William D. Emmons (November 18, 1924 – December 8, 2001) was an American chemist and published with William S. Wadsworth a modification to the Wittig-Horner reaction using phosphonate-stabilized carbanions, now called the Horner-Wadsworth-Emmons reaction or HWE reaction or Horner-Wittig reaction.
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Yohimbine
Yohimbine is an indole alkaloid derived from the bark of the Pausinystalia yohimbe tree in Central Africa.
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Sulfonyloxaziridine enolate oxidation.
References
[1] https://en.wikipedia.org/wiki/Oxaziridine
