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Reactions
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 |
|---|---|---|---|
| AMBIENT-TEMPERATURE ULLMAN REACTION: 4,5,4',5'-TETRAMETHOXY-1,1'-BIPHENYL-2,2'-DICARBOXALDEHYDE (1,1'-Biphenyl]-2,2'-dicarboxaldehyde, 4,4',5,5'-tetramethoxy-) | Preparation of 1,1'-Biphenyl]-2,2'-dicarboxaldehyde, 4,4',5,5'-tetramethoxy-. Submitted by F. E. Ziegler, K. W. Fowler, W. B. Rodgers, and R. T. Wester1. DOI: 10.15227/orgsyn.065.0108. | Organic Syntheses | |
| AMIDE FORMATION BY DECARBOXYLATIVE CONDENSATION OF HYDROXYLAMINES AND α-KETOACIDS: N-[(1S)-1 PHENYLETHYL]-BENZENEACETAMIDE Condensation | Preparation of AMIDE FORMATION BY DECARBOXYLATIVE CONDENSATION OF HYDROXYLAMINES AND α-KETOACIDS: N-[(1S)-1 PHENYLETHYL]-BENZENEACETAMIDE. Submitted by Lei Ju and Jeffrey W. Bode1. DOI: 10.15227/orgsy… | Organic Syntheses | |
| AMINES FROM MIXED CARBOXYLIC-CARBONIC ANHYDRIDES: 1-PHENYLCYCLOPENTYLAMINE (Cyclopentanamine, 1-phenyl-) | Preparation of Cyclopentanamine, 1-phenyl-. Submitted by Carl Kaiser and Joseph Weinstock1. DOI: 10.15227/orgsyn.051.0048. | Organic Syntheses | |
| AMINOACETAL (Acetaldehyde, amino-, diethyl acetal) | Preparation of Acetaldehyde, amino-, diethyl acetal. Submitted by R. B. Woodward and W. E. Doering. DOI: 10.15227/orgsyn.024.0003. | Organic Syntheses | |
| AMINOACETONE SEMICARBAZONE HYDROCHLORIDE (Amino-2-propanone, semicarbazone hydrochloride) | Preparation of Amino-2-propanone, semicarbazone hydrochloride. Submitted by John D. Hepworth1. DOI: 10.15227/orgsyn.045.0001. | Organic Syntheses | |
| AMINOGUANIDINE BICARBONATE (Guanidine, amino-, bicarbonate) | Preparation of Guanidine, amino-, bicarbonate. Submitted by R. L. Shriner and Fred W. Neumann. DOI: 10.15227/orgsyn.026.0007. | Organic Syntheses | |
| AMINOMALONONITRILE p-TOLUENESULFONATE (Malononitrile, amino-, p-toluenesulfonate) | Preparation of Malononitrile, amino-, p-toluenesulfonate. Submitted by J. P. Ferris, R. A. Sanchez, and R. W. Mancuso1. DOI: 10.15227/orgsyn.048.0001. | Organic Syntheses | |
| AMMONIUM SALT OF AURIN TRICARBOXYLIC ACID | Preparation of AMMONIUM SALT OF AURIN TRICARBOXYLIC ACID. Submitted by G. B. Heisig and W. M. Lauer. DOI: 10.15227/orgsyn.009.0008. | Organic Syntheses | |
| Andrussow process | The Andrussow process is the dominant industrial process for the production of hydrogen cyanide. It involves the reaction of methane, ammonia, and oxygen. The process is catalyzed by a platinum-rhodi… | Wikipedia: Category:Name reactions | |
| (+)- AND (−)-α-(2,4,5,7-TETRANITRO-9-FLUORENYLIDENEAMINOOXY)PROPIONIC ACID (Propionic acid, 2-(2,4,5,7-tetranitrofluoren-9-ylideneaminooxy)-, (+)- and (−)-) | Preparation of Propionic acid, 2-(2,4,5,7-tetranitrofluoren-9-ylideneaminooxy)-, (+)- and (−)-. Submitted by Paul Block Jr1 and Melvin S. Newman2. DOI: 10.15227/orgsyn.048.0120. | Organic Syntheses | |
| AN ECONOMICAL SYNTHESIS OF 4-TRIMETHYLSILYL-2-BUTYN-1-OL | Preparation of AN ECONOMICAL SYNTHESIS OF 4-TRIMETHYLSILYL-2-BUTYN-1-OL. Submitted by Alexander N. Wein, Rongbiao Tong, and Frank E. McDonald.1. DOI: 10.15227/orgsyn.088.0296. | Organic Syntheses | |
| An Efficient and Scalable Ritter Reaction for the Synthesis of t-Butyl Amides | Preparation of An Efficient and Scalable Ritter Reaction for the Synthesis of t-Butyl Amides. Submitted by Jacqueline E. Milne and Jean C. Baum1. DOI: 10.15227/orgsyn.089.0519. | Organic Syntheses | |
| AN EFFICIENT, HIGHLY DIASTEREO- AND ENANTIOSELECTIVE HETERO-DIELS-ALDER CATALYST. PREPARATION OF (2S,6R)-6-(tert-BUTYLDIMETHYL-SILYLOXYMETHYL)-2-METHOXY-2,5-DIHYDROPYRAN ((Silane, [[(2R,6S)-3,6-dihydro-6-methoxy-2H-pyran-2-yl]methoxy]-(1,1-dimethylethyl)dimethyl)-) | Preparation of (Silane, [[(2R,6S)-3,6-dihydro-6-methoxy-2H-pyran-2-yl]methoxy]-(1,1-dimethylethyl)dimethyl)-. Submitted by David E. Chavez and Eric N. Jacobsen1. DOI: 10.15227/orgsyn.082.0034. | Organic Syntheses | |
| A NEW PRACTICAL ONE-POT CONVERSION OF PHENOLS TO ANILINES: 6-AMINO-3,4-DIHYDRO-1(2H)-NAPHTHALENONE (1(2H)-Naphthalenone, 6-amino-3,4-dihydro-) | Preparation of 1(2H)-Naphthalenone, 6-amino-3,4-dihydro-. Submitted by Masahiro Mizuno1 and Mitsuhisa Yamano1. DOI: 10.15227/orgsyn.084.0325. | Organic Syntheses | |
| A NEW REAGENT FOR tert-BUTOXYCARBONYLATION: 2-tert-BUTOXYCARBONYLOXYIMINO-2-PHENYLACETONITRILE (Benzeneacetonitrile, α-[[[(1,1-dimethylethoxy)carbonyl]carbonyl]oxy]imino]-) | Preparation of Benzeneacetonitrile, α-[[[(1,1-dimethylethoxy)carbonyl]carbonyl]oxy]imino]-. Submitted by Masumi Itoh, Daijiro Hagiwara, and Takashi Kamiya1. DOI: 10.15227/orgsyn.059.0095. | Organic Syntheses | |
| Angeli–Rimini reaction | The Angeli–Rimini reaction is an organic reaction between an aldehyde and N-hydroxybenzenesulfonamide in presence of base forming a hydroxamic acid. | Wikipedia: Category:Name reactions | |
| ANHYDRO-2-HYDROXYMERCURI-3-NITROBENZOIC ACID (Benzoic acid, anhydro-2-hydroxymercuri-3-nitro-) | Preparation of Benzoic acid, anhydro-2-hydroxymercuri-3-nitro-. Submitted by Frank C. Whitmore, P. J. Culhane, and H. T. Neher. DOI: 10.15227/orgsyn.007.0001. | Organic Syntheses | |
| Anhydrous Hydration of Nitriles to Amides: p-Carbomethoxybenzamide | Preparation of Anhydrous Hydration of Nitriles to Amides: p-Carbomethoxybenzamide. Submitted by Dahye Kang, Jinwoo Lee, and Hee-Yoon Lee1. DOI: 10.15227/orgsyn.089.0066. | Organic Syntheses | |
| AN IMPROVED PREPARATION OF 3-BROMO-2H-PYRAN-2-ONE: AN AMBIPHILIC DIENE FOR DIELS-ALDER CYCLOADDITIONS (2H-Pyran-2-one, 3-bromo-) Cycloaddition | Preparation of 2H-Pyran-2-one, 3-bromo-. Submitted by G. H. Posner, K. Afarinkia, and H. Dai1. DOI: 10.15227/orgsyn.073.0231. | Organic Syntheses | |
| AN INTRAMOLECULAR AMINATION OF ARYL HALIDES WITH A COMBINATION OF COPPER (I) IODIDE AND CESIUM ACETATE: PREPARATION OF 5,6-DIMETHOXYINDOLE-1,2-DICARBOXYLIC ACID 1-BENZYL ESTER 2-METHYL ESTER | Preparation of AN INTRAMOLECULAR AMINATION OF ARYL HALIDES WITH A COMBINATION OF COPPER (I) IODIDE AND CESIUM ACETATE: PREPARATION OF 5,6-DIMETHOXYINDOLE-1,2-DICARBOXYLIC ACID 1-BENZYL ESTER 2-METHYL … | Organic Syntheses | |
| ANISOLE | Preparation of ANISOLE. Submitted by G. S. Hiers and F. D. Hager. DOI: 10.15227/orgsyn.009.0012. | Organic Syntheses | |
| ANODIC OXIDATION OF ACIDS: DIMETHYL DECANEDIOATE (Decanedioic acid, dimethyl ester) Oxidation | Preparation of Decanedioic acid, dimethyl ester. Submitted by D. A. White1. DOI: 10.15227/orgsyn.060.0001. | Organic Syntheses | |
| ANODIC OXIDATION OF N-CARBOMETHOXYPYRROLIDINE: 2-METHOXY-N-CARBOMETHOXYPYRROLIDINE (1-Pyrrolidinecarboxylic acid, 2-methoxy-, methyl ester) Oxidation | Preparation of 1-Pyrrolidinecarboxylic acid, 2-methoxy-, methyl ester. Submitted by T. Shono, Y. Matsumura, and K. Tsubata1. DOI: 10.15227/orgsyn.063.0206. | Organic Syntheses | |
| ANTHRONE | Preparation of ANTHRONE. Submitted by Kurt H. Meyer. DOI: 10.15227/orgsyn.008.0008. | Organic Syntheses | |
| ANTI-SELECTIVE BORON-MEDIATED ASYMMETRIC ALDOL REACTION OF CARBOXYLIC ESTERS: SYNTHESIS OF (2S, 3R)-2,4-DIMETHYL-1,3-PENTANEDIOL (1,3-Pentanediol, 2,4-dimethyl-, [S-(R*,S*)-) Condensation | Preparation of 1,3-Pentanediol, 2,4-dimethyl-, [S-(R*,S*)-. Submitted by Atsushi Abiko1. DOI: 10.15227/orgsyn.079.0116. | Organic Syntheses | |
| APPARATUS FOR CATALYTIC REDUCTION Reduction | Preparation of APPARATUS FOR CATALYTIC REDUCTION. Submitted by Roger Adams and V. Voorhees. DOI: 10.15227/orgsyn.008.0010. | Organic Syntheses | |
| Appel reaction Substitution | The Appel reaction is an organic reaction that converts an alcohol into an alkyl chloride using triphenylphosphine and carbon tetrachloride. The use of carbon tetrabromide or bromine as a halide sourc… | Wikipedia: Category:Name reactions | |
| A PRACTICAL AND SAFE PREPARATION OF 3,5-BIS(TRIFLUOROMETHYL)ACETOPHENONE (1-[3,5-Bis(trifluoromethyl)phenyl]-ethanone) | Preparation of 1-[3,5-Bis(trifluoromethyl)phenyl]-ethanone. Submitted by Johnnie L. Leazer Jr. and Raymond Cvetovich1. DOI: 10.15227/orgsyn.082.0115. | Organic Syntheses | |
| A PRACTICAL AND SCALABLE SYNTHESIS OF N-HALO COMPOUNDS: 2-CHLORO-6,7-DIMETHOXY-1,2,3,4-TETRAHYDROISOQUINOLINE | Preparation of A PRACTICAL AND SCALABLE SYNTHESIS OF N-HALO COMPOUNDS: 2-CHLORO-6,7-DIMETHOXY-1,2,3,4-TETRAHYDROISOQUINOLINE. Submitted by Yong-Li Zhong1 and Paul G. Bulger. DOI: 10.15227/orgsyn.087.0… | Organic Syntheses | |
| A PRACTICAL PROCEDURE FOR CARBONYL α-OXIDATION: SYNTHESIS OF (2-BENZOYLOXY)-1,4-CYCLOHEXANEDIONE MONO-ETHYLENE KETAL Oxidation | Preparation of A PRACTICAL PROCEDURE FOR CARBONYL α-OXIDATION: SYNTHESIS OF (2-BENZOYLOXY)-1,4-CYCLOHEXANEDIONE MONO-ETHYLENE KETAL. Submitted by Teyrnon C. Jones and Nicholas C. O. Tomkinson1. DOI: 1… | Organic Syntheses | |
| A Practical Synthesis of Isocyanates from Isonitriles: Ethyl 2-Isocyanatoacetate | Preparation of A Practical Synthesis of Isocyanates from Isonitriles: Ethyl 2-Isocyanatoacetate. Submitted by Hoang V. Le and Bruce Ganem1. DOI: 10.15227/orgsyn.089.0404. | Organic Syntheses | |
| APROTIC DOUBLE MICHAEL ADDITION: 1,3-DIMETHYL-5-OXOBICYCLO[2.2.2]OCTANE-2-CARBOXYLIC ACID (Bicyclo[2.2.2]octane-2-carboxylic acid, 1,3-dimethyl-5-oxo-) Addition | Preparation of Bicyclo[2.2.2]octane-2-carboxylic acid, 1,3-dimethyl-5-oxo-. Submitted by Dietrich Spitzner and Anita Engler1. DOI: 10.15227/orgsyn.066.0037. | Organic Syntheses | |
| ARENE OXIDE SYNTHESIS: PHENANTHRENE-9,10-OXIDE (Phenanthro[9,10-b]oxirene, 1a,9b-dihydro-) | Preparation of Phenanthro[9,10-b]oxirene, 1a,9b-dihydro-. Submitted by Cecilia Cortez and Ronald G. Harvey1. DOI: 10.15227/orgsyn.058.0012. | Organic Syntheses | |
| Arens–van Dorp synthesis | The Arens–van Dorp synthesis is a name reaction in organic chemistry. It describes the addition of lithiated ethoxyacetylenes to ketones to give propargyl alcohols, which can undergo further reaction … | Wikipedia: Category:Name reactions | |
| Arndt–Eistert reaction | In organic chemistry, the Arndt–Eistert reaction is the conversion of a carboxylic acid to its homologue. It is named for the German chemists Fritz Arndt (1885–1969) and Bernd Eistert (1902–1978). The… | Wikipedia: Category:Name reactions | |
| AROMATIC ALDEHYDES. MESITALDEHYDE (Benzaldehyde, 2,4,6-trimethyl-) | Preparation of Benzaldehyde, 2,4,6-trimethyl-. Submitted by A. Rieche, H. Gross, and E. Höft1. DOI: 10.15227/orgsyn.047.0001. | Organic Syntheses | |
| AROMATIC HYDROCARBONS FROM AROMATIC KETONES AND ALDEHYDES: 1,1-DIPHENYLETHANE (Benzene, 1-phenylethyl-) | Preparation of Benzene, 1-phenylethyl-. Submitted by Sharon D. Lipsky and Stan S. Hall1. DOI: 10.15227/orgsyn.055.0007. | Organic Syntheses | |
| ARSANILIC ACID | Preparation of ARSANILIC ACID. Submitted by W. Lee Lewis and H. C. Cheetham. DOI: 10.15227/orgsyn.003.0013. | Organic Syntheses | |
| ARSONO- AND ARSENOACETIC ACIDS (Acetic acid, arsono-, and Acetic acid, arsenodi-) | Preparation of Acetic acid, arsono-, and Acetic acid, arsenodi-. Submitted by C. S. Palmer. DOI: 10.15227/orgsyn.004.0005. | Organic Syntheses | |
| ar-TETRAHYDRO-α-NAPHTHOL (1-Naphthol, 5,6,7,8-tetrahydro-) | Preparation of 1-Naphthol, 5,6,7,8-tetrahydro-. Submitted by C. David Gutsche and Hugo H. Peter1. DOI: 10.15227/orgsyn.037.0080. | Organic Syntheses | |
| ARYLBENZENES: 3,4-DICHLOROBIPHENYL (Biphenyl, 3,4-dichloro-) | Preparation of Biphenyl, 3,4-dichloro-. Submitted by D. H. Hey and M. J. Perkins1. DOI: 10.15227/orgsyn.049.0044. | Organic Syntheses | |
| ARYLUREASI. CYANATE METHODp-BROMOPHENYLUREA (Urea, (p-bromophenyl)-) | Preparation of Urea, (p-bromophenyl)-. Submitted by Frederick Kurzer1. DOI: 10.15227/orgsyn.031.0008. | Organic Syntheses | |
| ARYLUREASII. UREA METHODp-ETHOXYPHENYLUREA (Dulcin) | Preparation of Dulcin. DOI: 10.15227/orgsyn.031.0011. | Organic Syntheses | |
| A SELECTIVE, HETEROGENEOUS OXIDATION USING A MIXTURE OF POTASSIUM PERMANGANATE AND CUPRIC SULFATE: (3aS,7aR)-HEXAHYDRO-(3S,6R)-DIMETHYL-2(3H)-BENZOFURANONE (2(3H)-Benzofuranone, hexahydro-3,6-dimethyl-, [3R-(3α,3aβ,6β,7aα)]-) Oxidation | Preparation of 2(3H)-Benzofuranone, hexahydro-3,6-dimethyl-, [3R-(3α,3aβ,6β,7aα)]-. Submitted by Charles W. Jefford, Yun Li, and Ying Wang1. DOI: 10.15227/orgsyn.071.0207. | Organic Syntheses | |
| A SIMPLE AND CONVENIENT METHOD FOR THE OXIDATION OF ORGANOBORANES USING SODIUM PERBORATE: (+)-ISOPINOCAMPHEOL (Bicyclo[3.1.1]heptan-3-ol, 2,6,6-trimethyl-, [1S-(1α,2β,3α,5α)]-) Oxidation | Preparation of Bicyclo[3.1.1]heptan-3-ol, 2,6,6-trimethyl-, [1S-(1α,2β,3α,5α)]-. Submitted by George W. Kabalka, John T. Maddox, Timothy Shoup, and Karla R. Bowers1. DOI: 10.15227/orgsyn.073.0116. | Organic Syntheses | |
| A SIMPLE AND CONVENIENT METHOD FOR THE PREPARATION OF (Z)-β-IODOACROLEIN AND OF (Z)- OR (E)-γ-IODO ALLYLIC ALCOHOLS: (Z)- AND (E)-1-IODOHEPT-1-EN-3-OL (2-Propenal, 3-iodo-, (Z)- and 1-Hepten-3-ol, 1-iodo-, (Z)- and (E)-) | Preparation of 2-Propenal, 3-iodo-, (Z)- and 1-Hepten-3-ol, 1-iodo-, (Z)- and (E)-. Submitted by Ilane Marek, Christophe Meyer, and Jean-F. Normant1. DOI: 10.15227/orgsyn.074.0194. | Organic Syntheses | |
| Asinger reaction | The Asinger reaction (sometimes referred to as the Asinger-4 component reaction or A-4CR for short) is a multicomponent reaction for the synthesis of 3-thiazolines and other related heterocycles. It i… | Wikipedia: Category:Name reactions | |
| A STABLE CHIRAL 1,4-DIHYDROPYRIDINE EQUIVALENT FOR THE ASYMMETRIC SYNTHESIS OF SUBSTITUTED PIPERIDINES: 2-CYANO-6-PHENYLOXAZOLOPIPERIDINE (5H-Oxazolo[3,2-a]pyridine-5-carbonitrile, hexahydro-3-phenyl-, [3R-(3α,5β,8aβ]) | Preparation of 5H-Oxazolo[3,2-a]pyridine-5-carbonitrile, hexahydro-3-phenyl-, [3R-(3α,5β,8aβ]. Submitted by Martine Bonin, David S. Grierson, Jacques Royer, and Henri-Philippe Husson1. DOI: 10.15227/o… | Organic Syntheses | |
| Aston–Greenburg rearrangement Rearrangement | The Aston–Greenburg rearrangement is a name reaction in organic chemistry. It allows for the generation of tertiary α-alkylesters from corresponding α-haloketones through a 1,2-rearrangement, with the… | Wikipedia: Category:Name reactions | |
| asym-DIMETHYLUREA (Urea, 1,1-dimethyl-) | Preparation of Urea, 1,1-dimethyl-. Submitted by Frederick Kurzer1. DOI: 10.15227/orgsyn.032.0061. | Organic Syntheses |
