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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 |
|---|---|---|---|
| BENZOYL FLUORIDE | Preparation of BENZOYL FLUORIDE. Submitted by George A. Olah and Stephen J. Kuhn1. DOI: 10.15227/orgsyn.045.0003. | Organic Syntheses | |
| BENZOYLFORMIC ACID (Glyoxylic acid, phenyl-) | Preparation of Glyoxylic acid, phenyl-. Submitted by T. S. Oakwood and C. A. Weisgerber. DOI: 10.15227/orgsyn.024.0016. | Organic Syntheses | |
| BENZOYL PIPERIDINE (Piperidine, 1-benzoyl-) | Preparation of Piperidine, 1-benzoyl-. Submitted by C. S. Marvel and W. A. Lazier. DOI: 10.15227/orgsyn.009.0016. | Organic Syntheses | |
| BENZYLACETOPHENONE (Propiophenone, β-phenyl-) | Preparation of Propiophenone, β-phenyl-. Submitted by Roger Adams, J. W. Kern, and R. L. Shriner. DOI: 10.15227/orgsyn.008.0036. | Organic Syntheses | |
| BENZYL ALCOHOL AS AN ALKYLATING AGENT USING THE RUTHENIUM-CATALYZED BORROWING HYDROGEN STRATEGY (4,4-Dimethyl-3-oxo-2-benzylpentanenitrile) | Preparation of 4,4-Dimethyl-3-oxo-2-benzylpentanenitrile. Submitted by Tracy D. Nixon, Paul A. Slatford, Michael K. Whittlesey, and Jonathan M. J. Williams1. DOI: 10.15227/orgsyn.086.0028. | Organic Syntheses | |
| BENZYLANILINE (Benzylamine, N-phenyl-) | Preparation of Benzylamine, N-phenyl-. Submitted by F. G. Willson and T. S. Wheeler. DOI: 10.15227/orgsyn.008.0038. | Organic Syntheses | |
| BENZYL BENZOATE (Benzoic acid, benzyl ester) | Preparation of Benzoic acid, benzyl ester. Submitted by O. Kamm and W. F. Kamm. DOI: 10.15227/orgsyn.002.0005. | Organic Syntheses | |
| BENZYL CHLOROMETHYL ETHER (Benzene, (chloromethyoxy)methyl-) | Preparation of Benzene, (chloromethyoxy)methyl-. Submitted by D. S. Connor1,2, G. W. Klein13, G. N. Taylor14, R. K. Boeckman, Jr.5, and J. B. Medwid6. DOI: 10.15227/orgsyn.052.0016. | Organic Syntheses | |
| BENZYL CHLOROMETHYL KETONE (2-Propanone, 1-chloro-3-phenyl-) | Preparation of 2-Propanone, 1-chloro-3-phenyl-. Submitted by Warren D. McPhee and Erwin Klingsberg. DOI: 10.15227/orgsyn.026.0013. | Organic Syntheses | |
| BENZYL CYANIDE (α-Tolunitrile) | Preparation of α-Tolunitrile. Submitted by Roger Adams and A. F. Thal. DOI: 10.15227/orgsyn.002.0009. | Organic Syntheses | |
| BENZYL ISOPROPOXYMETHYL CARBAMATE - AN AMINOMETHYLATING REAGENT FOR MANNICH REACTIONS OF TITANIUM ENOLATES Addition | Preparation of BENZYL ISOPROPOXYMETHYL CARBAMATE - AN AMINOMETHYLATING REAGENT FOR MANNICH REACTIONS OF TITANIUM ENOLATES. Submitted by Hartmut Meyer1, Albert K. Beck2, Radovan Sebesta2, and Dieter Se… | Organic Syntheses | |
| BENZYL PHTHALIMIDE (Phthalimide, N-benzyl-) | Preparation of Phthalimide, N-benzyl-. Submitted by Richard H. F. Manske. DOI: 10.15227/orgsyn.012.0010. | Organic Syntheses | |
| BENZYLTRIMETHYLAMMONIUM ETHOXIDE (Ammonium, benzyltrimethyl-, ethoxide) | Preparation of Ammonium, benzyltrimethyl-, ethoxide. Submitted by W. J. Croxall, Marion F. Fegley, and H. J. Schneider1. DOI: 10.15227/orgsyn.038.0005. | Organic Syntheses | |
| Bergman cyclization Cyclization | The Masamune-Bergman cyclization or Masamune-Bergman reaction or Masamune-Bergman cycloaromatization is an organic reaction and more specifically a rearrangement reaction taking place when an enediyne… | Wikipedia: Category:Name reactions | |
| Bergmann azlactone peptide synthesis | The Bergmann azlactone peptide synthesis is a classic organic synthesis process for the preparation of dipeptides. | Wikipedia: Category:Name reactions | |
| Bergmann degradation | The Bergmann degradation is a series of chemical reactions designed to remove a single amino acid from the carboxylic acid (C-terminal) end of a peptide. First demonstrated by Max Bergmann in 1934, it… | Wikipedia: Category:Name reactions | |
| Bernthsen acridine synthesis | The Bernthsen acridine synthesis is the chemical reaction of a diarylamine heated with a carboxylic acid (or acid anhydride) and zinc chloride to form a 9-substituted acridine. | Wikipedia: Category:Name reactions | |
| BETAINE HYDRAZIDE HYDROCHLORIDE (Girard’s Reagent) | Preparation of Girard’s Reagent. Submitted by André Girard. DOI: 10.15227/orgsyn.018.0010. | Organic Syntheses | |
| Betti reaction | The Betti reaction is a chemical addition reaction of aldehydes, primary aromatic amines and phenols producing α-aminobenzylphenols. | Wikipedia: Category:Name reactions | |
| BIALLYL (1,5-Hexadiene) | Preparation of 1,5-Hexadiene. Submitted by Amos Turk and Henry Chanan. DOI: 10.15227/orgsyn.027.0007. | Organic Syntheses | |
| BIARYLS FROM SIMPLE ARENES via ORGANOTELLURIUM INTERMEDIATES: 4,4'-DIMETHOXY-1,1'-BIPHENYL (1,1'-Biphenyl, 4,4'-dimethoxy-) | Preparation of 1,1'-Biphenyl, 4,4'-dimethoxy-. Submitted by J. Bergman1, R. Carlsson, and B. Sjöberg. DOI: 10.15227/orgsyn.057.0018. | Organic Syntheses | |
| BICYCLIC KETONES FOR THE SYNTHESIS OF TROPINOIDS: 2α,4α-DIMETHYL-8-OXABICYCLO[3.2.1]OCT-6-EN-3-ONE (8-Oxabicyclo[3.2.1]oct-6-en-3-one, 2α,4α-dimethyl-) | Preparation of 8-Oxabicyclo[3.2.1]oct-6-en-3-one, 2α,4α-dimethyl-. Submitted by M. R. Ashcroft and H. M. R. Hoffmann1. DOI: 10.15227/orgsyn.058.0017. | Organic Syntheses | |
| BICYCLO[1.1.0]BUTANE (Bicyclo[1.1.0]butane) | Preparation of Bicyclo[1.1.0]butane. Submitted by Gary M. Lampman and James C. Aumiller1. DOI: 10.15227/orgsyn.051.0055. | Organic Syntheses | |
| BICYCLO[2.1.0]PENT-2-ENE | Preparation of BICYCLO[2.1.0]PENT-2-ENE. Submitted by A. Harry Andrist, John E. Baldwin1, and Robert K. Pinschmidt, Jr. DOI: 10.15227/orgsyn.055.0015. | Organic Syntheses | |
| BICYCLO[2.1.0]PENTANE | Preparation of BICYCLO[2.1.0]PENTANE. Submitted by P. G. Gassman and K. T. Mansfield1. DOI: 10.15227/orgsyn.049.0001. | Organic Syntheses | |
| BICYCLO[2.2.1]HEPTEN-7-ONE (2-Norbornen-7-one) | Preparation of 2-Norbornen-7-one. Submitted by P. G. Gassman and J. L. Marshall1. DOI: 10.15227/orgsyn.048.0025. | Organic Syntheses | |
| BICYCLO[3.2.1]OCTAN-3-ONE (Bicyclo[3.2.1]octan-3-one) | Preparation of Bicyclo[3.2.1]octan-3-one. Submitted by C. W. Jefford1 2, J. Gunsher1, D. T. Hill1, P. Brun3, J. Le Gras3, and B. Waegell3. DOI: 10.15227/orgsyn.051.0060. | Organic Syntheses | |
| BICYCLOPROPYLIDENE (Cyclopropane, cyclopropylidene) | Preparation of Cyclopropane, cyclopropylidene. Submitted by Armin de Meijere, Sergei I. Kozhushkov, and Thomas Späth1. DOI: 10.15227/orgsyn.078.0142. | Organic Syntheses | |
| Biginelli reaction | The Biginelli reaction is a multiple-component chemical reaction that creates 3,4-dihydropyrimidin-2(1H)-ones 4 from ethyl acetoacetate 1, an aryl aldehyde (such as benzaldehyde 2), and urea 3. It is … | Wikipedia: Category:Name reactions | |
| Bimolecular Oxidative Amidation of Phenols: 1-(Acetylamino)-4-oxo-2,5-cyclohexadiene-1-acetic acid, Methyl Ester | Preparation of Bimolecular Oxidative Amidation of Phenols: 1-(Acetylamino)-4-oxo-2,5-cyclohexadiene-1-acetic acid, Methyl Ester. Submitted by Jaclyn Chau1 and Marco A. Ciufolini*1. DOI: 10.15227/orgsy… | Organic Syntheses | |
| Bingel reaction | The Bingel reaction in fullerene chemistry is a fullerene cyclopropanation reaction to a methanofullerene first discovered by C. Bingel in 1993 with the bromo derivative of diethyl malonate in the pr… | Wikipedia: Category:Name reactions | |
| Birch reduction Reduction | The Birch reduction or Metal-Ammonia reduction is an organic reaction that is used to convert arenes to 1,4-cyclohexadienes. The reaction is named after the Australian chemist Arthur Birch and involve… | Wikipedia: Category:Name reactions | |
| Birkeland–Eyde process | The Birkeland–Eyde process was one of the competing industrial processes in the beginning of nitrogen-based fertilizer production. It is a multi-step nitrogen fixation reaction that uses electrical ar… | Wikipedia: Category:Name reactions | |
| BIS(1,3-DIPHENYLIMIDAZOLIDINYLIDENE-2) (Δ2,2'-Bis(1,3-diphenylimidazolidine)) | Preparation of Δ2,2'-Bis(1,3-diphenylimidazolidine). Submitted by H.-W. Wanzlick1. DOI: 10.15227/orgsyn.047.0014. | Organic Syntheses | |
| BIS(2,2,2-TRICHLOROETHYL) AZODICARBOXYLATE (Diazenedicarboxylic acid, bis(2,2,2-trichloroethyl) ester) | Preparation of Diazenedicarboxylic acid, bis(2,2,2-trichloroethyl) ester. Submitted by R. Daniel Little and Manuel G. Venegas1, 2. DOI: 10.15227/orgsyn.061.0017. | Organic Syntheses | |
| BIS[2,2,2-TRIFLUORO-1-PHENYL-1-(TRIFLUOROMETHYL) ETHOXY] DIPHENYL SULFURANE (Sulfur, bis[α,α-bis(trifluoromethyl)benzenemethanolato]diphenyl-) | Preparation of Sulfur, bis[α,α-bis(trifluoromethyl)benzenemethanolato]diphenyl-. Submitted by J. C. Martin1, R. J. Arhart, J. A. Franz, E. F. Perozzi, and L. J. Kaplan. DOI: 10.15227/orgsyn.057.0022. | Organic Syntheses | |
| Bischler–Möhlau indole synthesis | The Bischler–Möhlau indole synthesis, also often referred to as the Bischler indole synthesis, is a chemical reaction that forms a 2-aryl-indole from an α-bromo-acetophenone and excess aniline; it is … | Wikipedia: Category:Name reactions | |
| Bischler–Napieralski reaction | The Bischler–Napieralski reaction is an intramolecular electrophilic aromatic substitution reaction that allows for the cyclization of β-arylethylamides or β-arylethylcarbamates. It was first discover… | Wikipedia: Category:Name reactions | |
| BISCHLOROMETHYL ETHER (Ether, bis(chloromethyl)-) | Preparation of Ether, bis(chloromethyl)-. Submitted by Saul R. Buc1. DOI: 10.15227/orgsyn.036.0001. | Organic Syntheses | |
| BIS(PINACOLATO)DIBORON (2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-) Rearrangement | Preparation of 2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-. Submitted by Tatsuo Ishiyama, Miki Murata, Taka-aki Ahiko, and Norio Miyaura1. DOI: 10.15227/orgsyn.077.0176. | Organic Syntheses | |
| BIS(TRIFLUOROETHYL) (CARBOETHOXYMETHYL)PHOSPHONATE (Acetic acid, [bis(2,2,2-trifluoroethoxy)phosphinyl]-, ethyl ester) | Preparation of Acetic acid, [bis(2,2,2-trifluoroethoxy)phosphinyl]-, ethyl ester. Submitted by Carl Patois1, Philippe Savignac1, Elie About-Jaudet2, and Noël Collignon2. DOI: 10.15227/orgsyn.073.0152. | Organic Syntheses | |
| BIS(TRIFLUOROMETHYL)DIAZOMETHANE (Propane, 2-diazo-1,1,1,3,3,3-hexafluoro-) | Preparation of Propane, 2-diazo-1,1,1,3,3,3-hexafluoro-. Submitted by W. J. Middleton1 and D. M. Gale. DOI: 10.15227/orgsyn.050.0006. | Organic Syntheses | |
| BIS(TRIMETHYLSILYL) PEROXIDE (BTMSPO) (Silane, dioxybis[trimethyl-) | Preparation of Silane, dioxybis[trimethyl-. Submitted by P. Dembech1, A. Ricci, G. Seconi, and M. Taddei. DOI: 10.15227/orgsyn.074.0084. | Organic Syntheses | |
| Blaise ketone synthesis | The Blaise ketone synthesis (named after Edmond Blaise) is the chemical reaction of acid chlorides with organozinc compounds to give ketones.[1][2] | Wikipedia: Category:Name reactions | |
| Blaise reaction | The Blaise reaction is an organic reaction that forms a β-ketoester from the reaction of zinc metal with an α-bromoester and a nitrile.[1][2][3] The reaction was first reported by Edmond Blaise (1872–… | Wikipedia: Category:Name reactions | |
| Blanc chloromethylation | The Blanc chloromethylation (also called the Blanc reaction) is the chemical reaction of aromatic rings with formaldehyde and hydrogen chloride to form chloromethyl arenes. The reaction is catalyzed … | Wikipedia: Category:Name reactions | |
| Blum–Ittah aziridine synthesis | The Blum–Ittah aziridine synthesis, also known as the Blum–Ittah-Shahak aziridine synthesis or simply the Blum aziridine synthesis is a name reaction of organic chemistry, for the generation of azirid… | Wikipedia: Category:Name reactions | |
| Bobbitt reaction | The Bobbitt reaction is a name reaction in organic chemistry. It is named after the American chemist James M. Bobbitt. The reaction allows the synthesis of 1-, 4-, and N-substituted 1,2,3,4-tetrahydro… | Wikipedia: Category:Name reactions | |
| Bodroux–Chichibabin aldehyde synthesis | The Bodroux–Chichibabin aldehyde synthesis is a chemical reaction whereby a Grignard reagent is converted to an aldehyde one carbon longer. | Wikipedia: Category:Name reactions | |
| Boekelheide reaction | The Boekelheide reaction is a rearrangement of α-picoline-N-oxides to hydroxymethylpyridines. It is named after Virgil Boekelheide who first reported it in 1954. Originally the reaction was carried ou… | Wikipedia: Category:Name reactions |
