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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 |
|---|---|---|---|
| dl-VALINE (Isovaleric acid, α-amino) | Preparation of Isovaleric acid, α-amino. Submitted by C. S. Marvel1. DOI: 10.15227/orgsyn.020.0106. | Organic Syntheses | |
| dl-α-AMINOPHENYLACETIC ACID (Glycine, α-phenyl-) | Preparation of Glycine, α-phenyl-. Submitted by Robert E. Steiger. DOI: 10.15227/orgsyn.022.0023. | Organic Syntheses | |
| dl-α-AMINO-α-PHENYLPROPIONIC ACID (Alanine, α-phenyl-, dl-) | Preparation of Alanine, α-phenyl-, dl-. Submitted by Robert E. Steiger. DOI: 10.15227/orgsyn.024.0009. | Organic Syntheses | |
| dl-β-AMINO-β-PHENYLPROPIONIC ACID (Hydrocinnamic acid, β-amino-dl-) | Preparation of Hydrocinnamic acid, β-amino-dl-. Submitted by Robert E. Steiger. DOI: 10.15227/orgsyn.022.0026. | Organic Syntheses | |
| dl-β-PHENYLALANINE (Alanine, β-phenyl-, dl-) | Preparation of Alanine, β-phenyl-, dl-. Submitted by H. B. Gillespie and H. R. Snyder. DOI: 10.15227/orgsyn.019.0067. | Organic Syntheses | |
| D-MANNOSE | Preparation of D-MANNOSE. Submitted by J. T. Sheehan and W. Freudenberg. DOI: 10.15227/orgsyn.022.0086. | Organic Syntheses | |
| DOCOSANEDIOIC ACID | Preparation of DOCOSANEDIOIC ACID. Submitted by S. Hünig, E. Lücke, and W. Brenninger1. DOI: 10.15227/orgsyn.043.0034. | Organic Syntheses | |
| Doebner–Miller reaction | The Doebner–Miller reaction is the organic reaction of an aniline with α,β-unsaturated carbonyl compounds to form quinolines. | Wikipedia: Category:Name reactions | |
| Doebner reaction | The Doebner reaction is the chemical reaction of an aniline with an aldehyde and pyruvic acid to form quinoline-4-carboxylic acids. | Wikipedia: Category:Name reactions | |
| Doering–LaFlamme allene synthesis | The Doering–LaFlamme allene synthesis is a reaction of alkenes that converts them to allenes by insertion of a carbon atom. This name reaction is named for William von Eggers Doering and a co-worker, … | Wikipedia: Category:Name reactions | |
| DOMINO DIELS–ALDER REACTION: 3,3a,3b,4,6a,7a-HEXAHYDRO-3,4,7-METHENO-7H-CYCLOPENTA[a]PENTALENE-7,8-DICARBOXYLIC ACID (3,4,7-Metheno-7H-cyclopenta[a]pentalene-7,8-dicarboxylic acid, 3,3a,3b,4,6a,7a-hexahydro) | Preparation of 3,4,7-Metheno-7H-cyclopenta[a]pentalene-7,8-dicarboxylic acid, 3,3a,3b,4,6a,7a-hexahydro. Submitted by Richard T. Taylor1, Michael W. Pelter1, and Leo A. Paquette2. DOI: 10.15227/orgsyn… | Organic Syntheses | |
| DOUBLE HYDROXYLATION REACTION FOR CONSTRUCTION OF THE CORTICOID SIDE CHAIN: 16α-METHYLCORTEXOLONE (Pregn-4-ene-3,20-dione, 17,21-dihydroxy-16-methyl-, (16α)-(±)-) | Preparation of Pregn-4-ene-3,20-dione, 17,21-dihydroxy-16-methyl-, (16α)-(±)-. Submitted by Yoshiaki Horiguchi, Eiichi Nakamura, and Isao Kuwajima1. DOI: 10.15227/orgsyn.073.0123. | Organic Syntheses | |
| Dowd–Beckwith ring-expansion reaction | The Dowd–Beckwith ring-expansion reaction is an organic reaction in which a cyclic carbonyl (typically a β-keto ester) is expanded by up to 4 carbons in a free radical ring expansion reaction through … | Wikipedia: Category:Name reactions | |
| Doyle–Kirmse reaction | The Doyle–Kirmse reaction is an organic reaction in which a metal carbene reacts with an allyl compound with transposition of the alkene and transfer of the electronegative group from the allyl onto t… | Wikipedia: Category:Name reactions | |
| D-(R)-GLYCERALDEHYDE ACETONIDE (1,3-Dioxolane-4-carboxaldehyde, 2,2-dimethyl-, (R)-) | Preparation of 1,3-Dioxolane-4-carboxaldehyde, 2,2-dimethyl-, (R)-. Submitted by Christopher R. Schmid and Jerry D. Bryant1. DOI: 10.15227/orgsyn.072.0006. | Organic Syntheses | |
| D-RIBONOLACTONE AND 2,3-ISOPROPYLIDENE(D-RIBONOLACTONE) (D-Ribonic acid, 2,3-O-(1-methylethylidene)-, γ-lactone) | Preparation of D-Ribonic acid, 2,3-O-(1-methylethylidene)-, γ-lactone. Submitted by John D. Williams1, Vivekanand P. Kamath2, Philip E. Morris2, and Leroy B. Townsend1. DOI: 10.15227/orgsyn.082.0075. | Organic Syntheses | |
| Duff reaction | The Duff reaction (after James Cooper Duff) also known as the hexamine aromatic formylation, is a formylation reaction used in organic chemistry for the synthesis of benzaldehydes. Hexamine acts as th… | Wikipedia: Category:Name reactions | |
| DURENE (By-products, penta- and hexamethylbenzene) | Preparation of By-products, penta- and hexamethylbenzene. Submitted by Lee Irvin Smith. DOI: 10.15227/orgsyn.010.0032. | Organic Syntheses | |
| DUROQUINONE | Preparation of DUROQUINONE. Submitted by Lee Irvin Smith. DOI: 10.15227/orgsyn.010.0040. | Organic Syntheses | |
| DYPNONE | Preparation of DYPNONE. Submitted by Winston Wayne and Homer Adkins. DOI: 10.15227/orgsyn.021.0039. | Organic Syntheses | |
| (E)-1-BENZYL-3-(1-IODOETHYLIDENE)PIPERIDINE: NUCLEOPHILE-PROMOTED ALKYNE-IMINIUM ION CYCLIZATIONS (Piperidine, 3-(iodoethylidene)-1-(phenylmethyl)-(E)-) Cyclization | Preparation of Piperidine, 3-(iodoethylidene)-1-(phenylmethyl)-(E)-. Submitted by H. Arnold, L. E. Overman, M. J. Sharp, and M. C. Witschel1. DOI: 10.15227/orgsyn.070.0111. | Organic Syntheses | |
| (E)-4-HEXEN-1-OL | Preparation of (E)-4-HEXEN-1-OL. Submitted by Raymond Paul, Olivier Riobé, and Michel Maumy1. DOI: 10.15227/orgsyn.055.0062. | Organic Syntheses | |
| Edman degradation | Edman degradation, developed by Pehr Edman, is a method of sequencing amino acids in a peptide. In this method, the amino-terminal residue is labeled and cleaved from the peptide without disrupting t… | Wikipedia: Category:Name reactions | |
| EFFICIENT ASYMMETRIC SYNTHESIS OF N-tert-BUTOXYCARBONYL α-AMINOACIDS USING 4-tert-BUTOXYCARBONYL- 5,6-DIPHENYLMORPHOLIN-2-ONE: (R)-(N-tert-BUTOXYCARBONYL)ALLYLGLYCINE ((4-Pentenoic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-, (2R)-)) | Preparation of (4-Pentenoic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-, (2R)-). Submitted by Robert M.Williams1, Peter J.Sinclair, and Duane E. DeMong. DOI: 10.15227/orgsyn.080.0031. | Organic Syntheses | |
| EFFICIENT ONE-POT SYNTHESIS OF BIS(4-TERT-BUTYLPHENYL)IODONIUM TRIFLATE | Preparation of EFFICIENT ONE-POT SYNTHESIS OF BIS(4-TERT-BUTYLPHENYL)IODONIUM TRIFLATE. Submitted by Marcin Bielawski and Berit Olofsson1. DOI: 10.15227/orgsyn.086.0308. | Organic Syntheses | |
| EFFICIENT OXIDATIVE SYNTHESIS OF (-)-2-TERT-BUTYL-(4S)-BENZYL-(1,3)-OXAZOLINE | Preparation of EFFICIENT OXIDATIVE SYNTHESIS OF (-)-2-TERT-BUTYL-(4S)-BENZYL-(1,3)-OXAZOLINE. Submitted by Björn T. Hahn, Kirsten Schwekendiek, and Frank Glorius1. DOI: 10.15227/orgsyn.085.0267. | Organic Syntheses | |
| EFFICIENT SYNTHESIS OF BROMIDES FROM CARBOXYLIC ACIDS CONTAINING A SENSITIVE FUNCTIONAL GROUP: DEC-9-ENYL BROMIDE FROM 10-UNDECENOIC ACID (1-Decene, 10-bromo-) | Preparation of 1-Decene, 10-bromo-. Submitted by Derek H. R. Barton1 , John MacKinnon, Roland N. Perchet, and Chi-Lam (Ivan) Tse. DOI: 10.15227/orgsyn.075.0124. | Organic Syntheses | |
| EFFICIENT SYNTHESIS OF HALOMETHYL-2,2'-BIPYRIDINES: 4,4'-BIS(CHLOROMETHYL)-2,2'-BIPYRIDINE (2,2'-Bipyridine, 4,4'-bis(chloromethyl)-) | Preparation of 2,2'-Bipyridine, 4,4'-bis(chloromethyl)-. Submitted by Adam P. Smith, Jaydeep J. S. Lamba, and Cassandra L. Fraser1. DOI: 10.15227/orgsyn.078.0082. | Organic Syntheses | |
| Efficient Synthesis of Oxime Using O-TBS-N-Tosylhydroxylamine: Preparation of (2Z)-4-(Benzyloxy)but-2-enal Oxime | Preparation of Efficient Synthesis of Oxime Using O-TBS-N-Tosylhydroxylamine: Preparation of (2Z)-4-(Benzyloxy)but-2-enal Oxime. Submitted by Katsushi Kitahara, Tatsuya Toma, and Jun Shimokawa and Toh… | Organic Syntheses | |
| Einhorn–Brunner reaction | The Einhorn–Brunner reaction is the designation for the chemical reaction of imides with alkyl hydrazines to form an isomeric mixture of 1,2,4-triazoles. It was initially described by the German chem… | Wikipedia: Category:Name reactions | |
| Elbs persulfate oxidation Oxidation | The Elbs persulfate oxidation is the organic reaction of phenols with alkaline potassium persulfate to form para-diphenols. The reaction is generally performed in water at room temperatures or below, … | Wikipedia: Category:Name reactions | |
| Elbs reaction | The Elbs reaction is an organic reaction describing the pyrolysis of an ortho methyl substituted benzophenone to a condensed polyaromatic. The reaction is named after its inventor, the German chemist … | Wikipedia: Category:Name reactions | |
| ELECTROHYDRODIMERIZATION OF AN ACTIVATED ALKENE: TETRAETHYL 1,2,3,4-BUTANETETRACARBOXYLATE (1,2,3,4-Butanetetracarboxylic acid, tetraethyl ester) | Preparation of 1,2,3,4-Butanetetracarboxylic acid, tetraethyl ester. Submitted by D. A. White1. DOI: 10.15227/orgsyn.060.0058. | Organic Syntheses | |
| ELECTROPHILIC CYCLIZATION WITH N-IODOSUCCINIMIDE: PREPARATION OF 5-(4-BROMOPHENYL)-3-IODO-2-(4-METHYL-PHENYL)FURAN Cyclization | Preparation of ELECTROPHILIC CYCLIZATION WITH N-IODOSUCCINIMIDE: PREPARATION OF 5-(4-BROMOPHENYL)-3-IODO-2-(4-METHYL-PHENYL)FURAN. Submitted by Adam Sniady, Marco S. Morreale, and Roman Dembinski1. DO… | Organic Syntheses | |
| ELECTROPHILIC N-AMINATION OF IMIDE SODIUM SALTS WITH O-DIPHENYLPHOSPHINYLHYDROXYLAMINE (DPH): 7-AMINOTHEOPHYLLINE (1H-Purine-2,6-dione, 7-amino-3,7-dihydro-1,3-dimethyl-) | Preparation of 1H-Purine-2,6-dione, 7-amino-3,7-dihydro-1,3-dimethyl-. Submitted by W. Klötzer, J. Stadlwieser, and J. Raneburger1. DOI: 10.15227/orgsyn.064.0096. | Organic Syntheses | |
| Emde degradation | The Emde degradation (also called Emde-reaction or Emde-reduction) is a method for the reduction of a quaternary ammonium cation to a tertiary amine with sodium amalgam: | Wikipedia: Category:Name reactions | |
| Enals via a Simple Two-Carbon Homologation of Aldehydes and Ketones | Preparation of Enals via a Simple Two-Carbon Homologation of Aldehydes and Ketones. Submitted by Petr Valenta, Natalie A. Drucker, and Patrick J. Walsh1. DOI: 10.15227/orgsyn.089.0527. | Organic Syntheses | |
| ENANTIOMERICALLY PURE ETHYL (R)- AND (S)- 2-FLUOROHEXANOATE BY ENZYME-CATALYZED KINETIC RESOLUTION (Hexanoic acid, 2-fluoro-, ethyl ester, (R)- and (S)-) | Preparation of Hexanoic acid, 2-fluoro-, ethyl ester, (R)- and (S)-. Submitted by P. Kalaritis and R. W. Regenye1. DOI: 10.15227/orgsyn.069.0010. | Organic Syntheses | |
| ENANTIOMERICALLY PURE β-AMINO ACIDS FROM 2-tert-BUTYL-1-CARBOMETHOXY-2,3-DIHYDRO-4(1H)-PYRIMIDINONE: (R)-3-AMINO-3-(p-METHOXYPHENYL)PROPIONIC ACID (1(2H)-Pyrimidinecarboxylic acid, 2-(1,1-dimethylethyl)-3,4-dihydro-4-oxo-, methyl ester, (R)- or (S)-) | Preparation of 1(2H)-Pyrimidinecarboxylic acid, 2-(1,1-dimethylethyl)-3,4-dihydro-4-oxo-, methyl ester, (R)- or (S)-. Submitted by F. J. Lakner, K. S. Chu, G. R. Negrete, and J. P. Konopelski1. DOI: 1… | Organic Syntheses | |
| ENANTIOMERIC (S)-(+)- AND (R)-(−)-1,1'-BINAPHTHYL-2,2'-DIYL HYDROGEN PHOSPHATE (Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin, 4-hydroxy-, 4-oxide) | Preparation of Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin, 4-hydroxy-, 4-oxide. Submitted by J. Jacques and C. Fouquey1. DOI: 10.15227/orgsyn.067.0001. | Organic Syntheses | |
| ENANTIOSELECTIVE ADDITION OF BUTYLLITHIUM IN THE PRESENCE OF THE CHIRAL COSOLVENT DDB: (R)-( + )-1-PHENYL-1-PENTANOL (Benzenemethanol, α-butyl-, (R)-) Addition | Preparation of Benzenemethanol, α-butyl-, (R)-. Submitted by Dieter Seebach and August Hidber1. DOI: 10.15227/orgsyn.061.0042. | Organic Syntheses | |
| Enantioselective Alkylation of 2-[(4-Chlorobenzyliden)Amino]Propanoic Acid tert-Butyl Ester: Synthesis of (R)-2-Amino-2-Methyl-3-Phenylpropanoic Acid tert-Butyl Ester | Preparation of Enantioselective Alkylation of 2-[(4-Chlorobenzyliden)Amino]Propanoic Acid tert-Butyl Ester: Synthesis of (R)-2-Amino-2-Methyl-3-Phenylpropanoic Acid tert-Butyl Ester. Submitted by Seij… | Organic Syntheses | |
| Enantioselective Alkylation of N-(Diphenylmethylene)glycinate tert-Butyl Ester: Synthesis of (R)-2-(Benzhydrylidenamino)-3-Phenylpropanoic Acid tert-Butyl Ester | Preparation of Enantioselective Alkylation of N-(Diphenylmethylene)glycinate tert-Butyl Ester: Synthesis of (R)-2-(Benzhydrylidenamino)-3-Phenylpropanoic Acid tert-Butyl Ester. Submitted by Seiji Shir… | Organic Syntheses | |
| ENANTIOSELECTIVE, CATALYTIC DIELS-ALDER REACTION: (1S-endo)-3-(BICYCLO[2.2.1]HEPT-5-EN-2-YLCARBONYL)-2-OXAZOLIDINONE (2-Oxazolidinone, 3-bicyclo[2.2.1]hept-5-en-2-ylcarbonyl)-, (1S-endo)-) | Preparation of 2-Oxazolidinone, 3-bicyclo[2.2.1]hept-5-en-2-ylcarbonyl)-, (1S-endo)-. Submitted by S. Pikul1 and E. J. Corey2. DOI: 10.15227/orgsyn.071.0030. | Organic Syntheses | |
| ENANTIOSELECTIVE EPOXIDATION OF ALLYLIC ALCOHOLS: (2S,3S)-3-PROPYLOXIRANEMETHANOL (Oxiranemethanol, 3-Propyl-, (2S,3S)-) Oxidation | Preparation of Oxiranemethanol, 3-Propyl-, (2S,3S)-. Submitted by J. Gordon Hill1, K. Barry Sharpless1, Christopher M. Exon2, and Ronald Regenye2. DOI: 10.15227/orgsyn.063.0066. | Organic Syntheses | |
| ENANTIOSELECTIVE HYDROLYSIS OF cis-3,5-DIACETOXYCYCLOPENTENE: (1R,4S)-(+)-4-HYDROXY-2-CYCLOPENTENYL ACETATE (4-Cyclopentene-1,3-diol, monoacetate, (1R-cis)-) Hydrolysis | Preparation of 4-Cyclopentene-1,3-diol, monoacetate, (1R-cis)-. Submitted by Donald R. Deardorff, Colin Q. Windham, and Chris L. Craney1. DOI: 10.15227/orgsyn.073.0025. | Organic Syntheses | |
| Enantioselective Nitroaldol (Henry) Reaction of p-Nitrobenzaldehyde and Nitromethane Using a Copper (II) Complex Derived from (R,R)-1,2-Diaminocyclohexane: (1S)-1-(4-Nitrophenyl)-2-nitroethane-1-ol Condensation | Preparation of Enantioselective Nitroaldol (Henry) Reaction of p-Nitrobenzaldehyde and Nitromethane Using a Copper (II) Complex Derived from (R,R)-1,2-Diaminocyclohexane: (1S)-1-(4-Nitrophenyl)-2-nitr… | Organic Syntheses | |
| Enantioselective Organocatalytic α-Arylation of Aldehydes | Preparation of Enantioselective Organocatalytic α-Arylation of Aldehydes. Submitted by Pernille H. Poulsen, Mette Overgaard, Kim L. Jensen and Karl Anker Jørgensen*1. DOI: 10.15227/orgsyn.091.0175. | Organic Syntheses | |
| ENANTIOSELECTIVE OXIDATION OF AN ALKYL ARYL SULFIDE: SYNTHESIS OF (S)-(-)-METHYL P-BROMOPHENYL SULFOXIDE Oxidation | Preparation of ENANTIOSELECTIVE OXIDATION OF AN ALKYL ARYL SULFIDE: SYNTHESIS OF (S)-(-)-METHYL P-BROMOPHENYL SULFOXIDE. Submitted by Carmelo Drago, Emma-Jane Walker, Lorenzo Caggiano, and Richard F. … | Organic Syntheses | |
| ENANTIOSELECTIVE OXIDATION OF A SULFIDE: (S)-(−)-METHYL p-TOLYL SULFOXIDE (Benzene, 1-methyl-4-(methylsulfinyl)-, (S)-) Oxidation | Preparation of Benzene, 1-methyl-4-(methylsulfinyl)-, (S)-. Submitted by S. H. Zhao, O. Samuel, and H. B. Kagan1. DOI: 10.15227/orgsyn.068.0049. | Organic Syntheses |
