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3374 reactions imported from Wikipedia named-reactions and Organic Syntheses archives. Filter by source or search by name + summary.
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| Equation | Name | Summary | Source |
|---|---|---|---|
| ASYMMETRIC ALCOHOLYSIS OF MESO-ANHYDRIDES MEDIATED BY ALKALOIDS (Bicyclo[2.2.1]hept-5-ene-2-endo-carboxylic acid, 3-endo-benzyloxycarbonyl, (2R,3S)-) | Preparation of Bicyclo[2.2.1]hept-5-ene-2-endo-carboxylic acid, 3-endo-benzyloxycarbonyl, (2R,3S)-. Submitted by Carsten Bolm1, Iuliana Atodiresei, and Ingo Schiffers. DOI: 10.15227/orgsyn.082.0120. | Organic Syntheses | |
| ASYMMETRIC CATALYTIC GLYOXYLATE-ENE REACTION: METHYL (2R)-2-HYDROXY-4-PHENYL-4-PENTENOATE (Benzenebutanoic acid, α-hydroxy-γ-methylene, methyl ester, (R)-) | Preparation of Benzenebutanoic acid, α-hydroxy-γ-methylene, methyl ester, (R)-. Submitted by Koichi Mikami, Masahiro Terada, Satoshi Narisawa, and Takeshi Nakai1. DOI: 10.15227/orgsyn.071.0014. | Organic Syntheses | |
| ASYMMETRIC EPOXIDATION OF trans-β-METHYLSTYRENE AND 1-PHENYLCYCLOHEXENE USING A D-FRUCTOSE-DERIVED KETONE: (R,R)-trans-β-METHYLSTYRENE OXIDE AND (R,R)-1-PHENYLCYCLOHEXENE OXIDE ((Oxirane, 2-methyl-3-phenyl-, (2R,3R)- and 7-Oxabicyclo[4.1.0]heptane,1-phenyl-)) Oxidation | Preparation of (Oxirane, 2-methyl-3-phenyl-, (2R,3R)- and 7-Oxabicyclo[4.1.0]heptane,1-phenyl-). Submitted by Zhi-Xian Wang, Lianhe Shu, Michael Frohn, Yong Tu, and Yian Shi1. DOI: 10.15227/orgsyn.080… | Organic Syntheses | |
| ASYMMETRIC HYDROBORATION OF 5-SUBSTITUTED CYCLOPENTADIENES: SYNTHESIS OF METHYL (1 R,5R)-5-HYDROXY-2-CYCLOPENTENE-1-ACETATE (2-Cyclopentene-1-acetic acid, 5-hydroxy-, methyl ester, (1R-trans)-) Addition | Preparation of 2-Cyclopentene-1-acetic acid, 5-hydroxy-, methyl ester, (1R-trans)-. Submitted by John J. Partridge, Naresh K. Chadha, and Milan R. Uskokovic1. DOI: 10.15227/orgsyn.063.0044. | Organic Syntheses | |
| ASYMMETRIC HYDROGENATION OF 3-OXO CARBOXYLATES USING BINAP-RUTHENIUM COMPLEXES: (R)-(−)-METHYL 3-HYDROXYBUTANOATE (Butanoic acid, 3-hydroxy-, methyl ester, (R)-) Reduction | Preparation of Butanoic acid, 3-hydroxy-, methyl ester, (R)-. Submitted by Masato Kitamura, Makoto Tokunaga, Takeshi Ohkuma, and Ryoji Noyori1. DOI: 10.15227/orgsyn.071.0001. | Organic Syntheses | |
| ASYMMETRIC HYDROGENATION OF ALLYLIC ALCOHOLS USING BINAP-RUTHENIUM COMPLEXES: (S)-(−)-CITRONELLOL (6-Octen-1-ol, 3,7-dimethyl, (S)-) Reduction | Preparation of 6-Octen-1-ol, 3,7-dimethyl, (S)-. Submitted by Hidemasa Takaya1, Tetsuo Ohta1, Shin-ichi Inoue2, Makoto Tokunaga2, Masato Kitamura2, and Ryoji Noyori2. DOI: 10.15227/orgsyn.072.0074. | Organic Syntheses | |
| ASYMMETRIC HYDROGENATION OF KETOPANTOYL LACTONE: D-(−)-PANTOYL LACTONE (2(3H)-Furanone, dihydro-3-hydroxy-4,4-dimethyl-) Reduction | Preparation of 2(3H)-Furanone, dihydro-3-hydroxy-4,4-dimethyl-. Submitted by I. Ojima, T. Kogure, and Y. Yoda1. DOI: 10.15227/orgsyn.063.0018. | Organic Syntheses | |
| ASYMMETRIC REARRANGEMENT OF ALLYLIC TRICHLOROACETIMIDATES: PREPARATION OF (S)-2,2,2-TRICHLORO-N-(1-PROPYLALLYL)ACETAMIDE (Acetamide, 2,2,2-trichloro-N-[(1S)-1-ethenylbutyl]-) Rearrangement | Preparation of Acetamide, 2,2,2-trichloro-N-[(1S)-1-ethenylbutyl]-. Submitted by Carolyn E. Anderson, Larry E. Overman*, and Mary P. Watson. DOI: 10.15227/orgsyn.082.0134. | Organic Syntheses | |
| ASYMMETRIC REDUCTION OF α,β-ACETYLENIC KETONES WITH B-3-PINANYL-9-BORABICYCLO[3.3.1]NONANE: (R)-( + )-1-OCTYN-3-OL (1-Octyn-3-ol, (R)-) Reduction | Preparation of 1-Octyn-3-ol, (R)-. Submitted by M. Mark Midland and Richard S. Graham1. DOI: 10.15227/orgsyn.063.0057. | Organic Syntheses | |
| ASYMMETRIC SYNTHESES USING THE SAMP-/RAMP-HYDRAZONE METHOD: (S)-(+)-4-METHYL-3-HEPTANONE (3-Heptanone, 4-methyl, (S)-) | Preparation of 3-Heptanone, 4-methyl, (S)-. Submitted by Dieter Enders, Helmut Kipphardt, and Peter Fey1. DOI: 10.15227/orgsyn.065.0183. | Organic Syntheses | |
| ASYMMETRIC SYNTHESIS OF 4,4-DIALKYLCYCLOHEXENONES FROM CHIRAL BICYCLIC LACTAMS: (R)-4-ETHYL-4-ALLYL-2-CYCLOHEXEN-1-ONE | Preparation of ASYMMETRIC SYNTHESIS OF 4,4-DIALKYLCYCLOHEXENONES FROM CHIRAL BICYCLIC LACTAMS: (R)-4-ETHYL-4-ALLYL-2-CYCLOHEXEN-1-ONE. Submitted by Albert I. Meyers and Daniel Berney1. DOI: 10.15227/o… | Organic Syntheses | |
| ASYMMETRIC SYNTHESIS OF DIETHYL (R)-(−)-(1-AMINO-3-METHYLBUTYL)PHOSPHONATE (Phosphonic acid, (1-amino-3-methylbutyl)-, diethyl ester, (R)-) | Preparation of Phosphonic acid, (1-amino-3-methylbutyl)-, diethyl ester, (R)-. Submitted by Amos B. Smith, III, Kraig M. Yager, Barton W. Phillips, and Carol M. Taylor1. DOI: 10.15227/orgsyn.075.0019. | Organic Syntheses | |
| ASYMMETRIC SYNTHESIS OF (M)-2-HYDROXYMETHYL-1-(2-HYDROXY-4,6-DIMETHYLPHENYL)NAPHTHALENE VIA A CONFIGURATIONALLY UNSTABLE BIARYL LACTONE (2-Naphthalenemethanol, 1-(2-hydroxy-4,6-dimethylphenyl)-, (R)-) | Preparation of 2-Naphthalenemethanol, 1-(2-hydroxy-4,6-dimethylphenyl)-, (R)-. Submitted by Gerhard Bringmann1 , Matthias Breuning, Petra Henschel, and Jürgen Hinrichs. DOI: 10.15227/orgsyn.079.0072. | Organic Syntheses | |
| ASYMMETRIC SYNTHESIS OF N-tert-BUTOXYCARBONYL α-AMINO ACIDS. SYNTHESIS OF (5S,6R)-4-tert-BUTOXYCARBONYL-5,6-DIPHENYLMORPHOLIN-2-ONE ((4-Morpholinecarboxylic acid, 6-oxo-2,3-diphenyl-, 1,1-dimethylethyl ester, (2S,3R)-)) | Preparation of (4-Morpholinecarboxylic acid, 6-oxo-2,3-diphenyl-, 1,1-dimethylethyl ester, (2S,3R)-). Submitted by Robert M. Williams, Peter J. Sinclair, Duane E. DeMong, Daimo Chen, and Dongguan Zhai… | Organic Syntheses | |
| ASYMMETRIC SYNTHESIS OF trans-2-AMINOCYCLOHEXANECARBOXYLIC ACID DERIVATIVES FROM PYRROLOBENZODIAZEPINE-5,11-DIONES: (1S,2S)-2-(N-TOSYLAMINO)CYCLOHEXANECARBOXYLIC ACID | Preparation of ASYMMETRIC SYNTHESIS OF trans-2-AMINOCYCLOHEXANECARBOXYLIC ACID DERIVATIVES FROM PYRROLOBENZODIAZEPINE-5,11-DIONES: (1S,2S)-2-(N-TOSYLAMINO)CYCLOHEXANECARBOXYLIC ACID. Submitted by Arth… | Organic Syntheses | |
| ASYMMETRIC SYNTHESIS OF α-AMINO ACIDS BY THE ALKYLATION OF PSEUDOEPHEDRINE GLYCINAMIDE: L-ALLYLGLYCINE AND N-BOC-L-ALLYLGLYCINE (Acetamide, 2-amino-N-(2-hydroxy-1-methyl-2-phenylethyl)-N-methyl-, [R-(R,R)]-, 4-Pentenoic acid, 2-amino-, (R)- and 4-Pentenoic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-, (R)-)) | Preparation of Acetamide, 2-amino-N-(2-hydroxy-1-methyl-2-phenylethyl)-N-methyl-, [R-(R,R)]-, 4-Pentenoic acid, 2-amino-, (R)- and 4-Pentenoic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-, (R)-). Su… | Organic Syntheses | |
| Atherton–Todd reaction | The Atherton-Todd reaction is a name reaction in organic chemistry, which goes back to the British chemists F. R. Atherton, H. T. Openshaw and A. R. Todd. These described the reaction for the first ti… | Wikipedia: Category:Name reactions | |
| ATROLACTIC ACID | Preparation of ATROLACTIC ACID. Submitted by Ernest L. Eliel and Jeremiah P. Freeman1. DOI: 10.15227/orgsyn.033.0007. | Organic Syntheses | |
| ATROPALDEHYDE (Benzeneacetaldehyde, α-methylene) | Preparation of Benzeneacetaldehyde, α-methylene. Submitted by Ingolf Crossland1. DOI: 10.15227/orgsyn.060.0006. | Organic Syntheses | |
| AU(I)-CATALYZED HYDRATION OF ALKYNES: 2,8-NONANEDIONE | Preparation of AU(I)-CATALYZED HYDRATION OF ALKYNES: 2,8-NONANEDIONE. Submitted by Eiichiro Mizushima,1 Dong-Mei Cui,1 Dilip Chandra Deb Nath,1 Teruyuki Hayashi,*1,2a and Masato Tanaka.1,2b. DOI: 10.1… | Organic Syntheses | |
| Auwers synthesis | The Auwers synthesis is a series of organic reactions forming a flavonol from a coumarone. This reaction was first reported by Karl von Auwers in 1908. | Wikipedia: Category:Name reactions | |
| A WATER-SOLUBLE TIN HYDRIDE: TRIS[3-(2-METHOXYETHOXY)PROPYL]STANNANE (2,5,13,16-Tetraoxa-9-stannaheptadecane, 9-[3-(2-methoxyethoxy)propyl]-) | Preparation of 2,5,13,16-Tetraoxa-9-stannaheptadecane, 9-[3-(2-methoxyethoxy)propyl]-. Submitted by James Light and Ronald Breslow1. DOI: 10.15227/orgsyn.072.0199. | Organic Syntheses | |
| A XANTHATE-TRANSFER APPROACH TO α-TRIFLUOROMETHYLAMINES (2-(N-ACETYLAMINO)-4,4-DIMETHOXY-1,1,1-TRIFLUOROBUTANE) | Preparation of 2-(N-ACETYLAMINO)-4,4-DIMETHOXY-1,1,1-TRIFLUOROBUTANE. Submitted by Fabien Gagosz and Samir Z. Zard1. DOI: 10.15227/orgsyn.084.0032. | Organic Syntheses | |
| Aza-Baylis–Hillman reaction | The aza-Baylis–Hillman reaction or aza-BH reaction in organic chemistry is a variation of the Baylis–Hillman reaction and describes the reaction of an electron deficient alkene, usually an α,β-unsatur… | Wikipedia: Category:Name reactions | |
| Aza-Cope rearrangement Rearrangement | Rearrangements, especially those that can participate in cascade reactions, such as the aza-Cope rearrangements, are of high practical as well as conceptual importance in organic chemistry, due to the… | Wikipedia: Category:Name reactions | |
| Aza-Diels–Alder reaction | The aza-Diels–Alder reaction is a modification of the Diels–Alder reaction wherein a nitrogen replaces sp2 carbon. The nitrogen atom can be part of the diene or the dienophile. | Wikipedia: Category:Name reactions | |
| Aza-Wittig reaction Olefination | The Aza-Wittig reaction or is a chemical reaction of a carbonyl group with an aza-ylide, also known as an iminophosphorane (R3P=NR'). Aza-Wittig reactions are most commonly used to convert aldehydes… | Wikipedia: Category:Name reactions | |
| AZELAIC ACID | Preparation of AZELAIC ACID. Submitted by Julian W. Hill and W. L. McEwen. DOI: 10.15227/orgsyn.013.0004. | Organic Syntheses | |
| AZELANITRILE | Preparation of AZELANITRILE. Submitted by Arthur C. Cope, Robert J. Cotter, and Leland L. Estes1. DOI: 10.15227/orgsyn.034.0004. | Organic Syntheses | |
| AZETIDINE | Preparation of AZETIDINE. Submitted by Donald H. Wadsworth1. DOI: 10.15227/orgsyn.053.0013. | Organic Syntheses | |
| Azide-alkyne Huisgen cycloaddition 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. Rolf Huisgen was the first to understand the scope of… | Wikipedia: Category:Name reactions | |
| AZIRIDINES FROM β-IODOCARBAMATES: 1,2,3,4-TETRAHYDRONAPHTHALENE(1,2)IMINE (1H-Naphth[1,2-b]azirine, 1a,2,3,7b-tetrahydro-) | Preparation of 1H-Naphth[1,2-b]azirine, 1a,2,3,7b-tetrahydro-. Submitted by C. H. Heathcock1 and A. Hassner2. DOI: 10.15227/orgsyn.051.0053. | Organic Syntheses | |
| AZLACTONE OF α-BENZOYLAMINO-β-(3,4-DIMETHOXYPHENYL)-ACRYLIC ACID (5(4)-Oxazolone, 2-phenyl-4-veratral-) | Preparation of 5(4)-Oxazolone, 2-phenyl-4-veratral-. Submitted by Johannes S. Buck and Walter S. Ide. DOI: 10.15227/orgsyn.013.0008. | Organic Syntheses | |
| AZOBENZENE | Preparation of AZOBENZENE. Submitted by H. E. Bigelow and D. B. Robinson. DOI: 10.15227/orgsyn.022.0028. | Organic Syntheses | |
| AZOETHANE (Diazene, diethyl) | Preparation of Diazene, diethyl. Submitted by Roland Ohme, Helmut Preuschhof, and Hans-Ulrich Heyne1. DOI: 10.15227/orgsyn.052.0011. | Organic Syntheses | |
| AZOXYBENZENE | Preparation of AZOXYBENZENE. Submitted by H. E. Bigelow and Albert Palmer. DOI: 10.15227/orgsyn.011.0016. | Organic Syntheses | |
| AZULENE | Preparation of AZULENE. Submitted by Klaus Hafner and Klaus-Peter Meinhardt1. DOI: 10.15227/orgsyn.062.0134. | Organic Syntheses | |
| Babler oxidation Oxidation | The Babler oxidation, also known as the Babler–Dauben oxidation, is an organic reaction for the oxidative transposition of tertiary allylic alcohols to enones using pyridinium chlorochromate (PCC): | Wikipedia: Category:Name reactions | |
| Baeyer–Drewsen indigo synthesis | The Baeyer–Drewsen indigo synthesis (1882) is an organic reaction in which indigo is prepared from 2-nitrobenzaldehyde and acetone The reaction was developed by von Baeyer and Viggo Drewsen in … | Wikipedia: Category:Name reactions | |
| Baeyer–Emmerling indole synthesis | Baeyer–Emmerling indole synthesis is a method for synthesizing indole from a (substituted) ortho-nitrocinnamic acid and iron powder in strongly basic solution. This reaction was discovered by Adolf vo… | Wikipedia: Category:Name reactions | |
| Baeyer–Villiger oxidation Oxidation | The Baeyer–Villiger oxidation is an organic reaction that forms an ester from a ketone or a lactone from a cyclic ketone, using peroxyacids or peroxides as the oxidant. The reaction is named after Ado… | Wikipedia: Category:Name reactions | |
| Bailey peptide synthesis | The Bailey peptide synthesis is a name reaction in organic chemistry developed 1949 by J. L. Bailey. It is a method for the synthesis of a peptide from α-amino acid-N-carboxylic acid anhydrides (NCAs)… | Wikipedia: Category:Name reactions | |
| Baker–Venkataraman rearrangement Rearrangement | The Baker–Venkataraman rearrangement is the chemical reaction of 2-acetoxyacetophenones with base to form 1,3-diketones. | Wikipedia: Category:Name reactions | |
| Balz–Schiemann reaction | The Balz–Schiemann reaction (also called the Schiemann reaction) is a chemical reaction in which an aryl diazonium salt is transformed to an aryl fluoride. This reaction is a traditional route to fluo… | Wikipedia: Category:Name reactions | |
| Bamberger rearrangement Rearrangement | The Bamberger rearrangement is the chemical reaction of phenylhydroxylamines with strong aqueous acid, which will rearrange to give 4-aminophenols. It is named for the German chemist Eugen Bamberger (… | Wikipedia: Category:Name reactions | |
| Bamberger triazine synthesis | The Bamberger triazine synthesis in organic chemistry is a classic organic synthesis of a triazine first reported by Eugen Bamberger in 1892. | Wikipedia: Category:Name reactions | |
| Bamford–Stevens reaction | The Bamford–Stevens reaction is a chemical reaction whereby treatment of tosylhydrazones with strong base gives alkenes. It is named for the British chemist William Randall Bamford and the Scottish ch… | Wikipedia: Category:Name reactions | |
| Banert cascade | The Banert cascade is an organic reaction in which an NH-1,2,3-triazole is prepared from a propargyl halide or sulfate and sodium azide in a dioxane- water mixture at elevated temperatures. It is name… | Wikipedia: Category:Name reactions | |
| Barbier reaction Organometallic addition | The Barbier reaction is an organometallic reaction between an alkyl halide (chloride, bromide, iodide), a carbonyl group and a metal. The reaction can be performed using magnesium, aluminium, zinc, in… | Wikipedia: Category:Name reactions | |
| Barbier–Wieland degradation Organometallic addition | The Barbier–Wieland degradation is a procedure for shortening the carbon chain of a carboxylic acid by one carbon. It only works when the carbon adjacent to the carboxyl is a simple methylene bridge (… | Wikipedia: Category:Name reactions |
