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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 |
|---|---|---|---|
| ALDEHYDES FROM 2-BENZYL-4,4,6-TRIMETHYL-5,6-DIHYDRO-1,3(4H)-OXAZINE: 1-PHENYLCYCLOPENTANECARBOXALDEHYDE (Cyclopentanecarboxaldehyde, 1-phenyl-) | Preparation of Cyclopentanecarboxaldehyde, 1-phenyl-. Submitted by Ieva R. Politzer and A. I. Meyers1. DOI: 10.15227/orgsyn.051.0024. | Organic Syntheses | |
| ALDEHYDES FROM 4,4-DIMETHYL-2-OXAZOLINE AND GRIGNARD REAGENTS: o-ANISALDEHYDE (Benzaldehyde, 2-methoxy-) Organometallic addition | Preparation of Benzaldehyde, 2-methoxy-. Submitted by R. S. Brinkmeyer, E. W. Collington, and A. I. Meyers1. DOI: 10.15227/orgsyn.054.0042. | Organic Syntheses | |
| ALDEHYDES FROM ACID CHLORIDES BY MODIFIED ROSENMUND REDUCTION: 3,4,5-TRIMETHOXYBENZALDEHYDE (Benzaldehyde, 3,4,5-trimethoxy-) Reduction | Preparation of Benzaldehyde, 3,4,5-trimethoxy-. Submitted by A. I. Rachlin, H. Gurien, and D. P. Wagner1. DOI: 10.15227/orgsyn.051.0008. | Organic Syntheses | |
| ALDEHYDES FROM ACID CHLORIDES BY REDUCTION OF ESTER-MESYLATES WITH SODIUM BOROHYDRIDE: CYCLOBUTANECARBOXALDEHYDE Reduction | Preparation of ALDEHYDES FROM ACID CHLORIDES BY REDUCTION OF ESTER-MESYLATES WITH SODIUM BOROHYDRIDE: CYCLOBUTANECARBOXALDEHYDE. Submitted by M. Ross Johnson and Bruce Rickborn1. DOI: 10.15227/orgsyn.… | Organic Syntheses | |
| ALDEHYDES FROM ALLYLIC ALCOHOLS AND PHENYLPALLADIUM ACETATE: 2-METHYL-3-PHENYLPROPIONALDEHYDE (Benzenepropanal, α-methyl-) | Preparation of Benzenepropanal, α-methyl-. Submitted by R. F. Heck1. DOI: 10.15227/orgsyn.051.0017. | Organic Syntheses | |
| ALDEHYDES FROM AROMATIC NITRILES: 4-FORMYLBENZENESULFONAMIDE (Benzenesulfonamide, 4-formyl-) | Preparation of Benzenesulfonamide, 4-formyl-. Submitted by T. van Es and B. Staskun1. DOI: 10.15227/orgsyn.051.0020. | Organic Syntheses | |
| ALDEHYDES FROM OLEFINS: CYCLOHEXANECARBOXALDEHYDE | Preparation of ALDEHYDES FROM OLEFINS: CYCLOHEXANECARBOXALDEHYDE. Submitted by P. Pino1 and C. Botteghi2. DOI: 10.15227/orgsyn.057.0011. | Organic Syntheses | |
| ALDEHYDES FROM PRIMARY ALCOHOLS BY OXIDATION WITH CHROMIUM TRIOXIDE: HEPTANAL Oxidation | Preparation of ALDEHYDES FROM PRIMARY ALCOHOLS BY OXIDATION WITH CHROMIUM TRIOXIDE: HEPTANAL. Submitted by J. C. Collins1 and W. W. Hess2. DOI: 10.15227/orgsyn.052.0005. | Organic Syntheses | |
| ALDEHYDES FROM sym-TRITHIANE: n-PENTADECANAL (Pentadecanal) | Preparation of Pentadecanal. Submitted by D. Seebach1 and A. K. Beck. DOI: 10.15227/orgsyn.051.0039. | Organic Syntheses | |
| Aldol–Tishchenko reaction Condensation | The Aldol–Tishchenko reaction is a tandem reaction involving an aldol reaction and a Tishchenko reaction. In organic synthesis, it is a method to convert aldehydes and ketones into 1,3-hydroxyl compou… | Wikipedia: Category:Name reactions | |
| Algar–Flynn–Oyamada reaction | The Algar–Flynn–Oyamada reaction is a chemical reaction whereby a chalcone undergoes an oxidative cyclization to form a flavonol. | Wikipedia: Category:Name reactions | |
| ALIPHATIC AND AROMATIC β-KETO ESTERS FROM MONOETHYL MALONATE: ETHYL 2-BUTYRYLACETATE (Pentanoic acid, 4-methyl-3-oxo-, ethyl ester) | Preparation of Pentanoic acid, 4-methyl-3-oxo-, ethyl ester. Submitted by W. Wierenga and H. I. Skulnick1. DOI: 10.15227/orgsyn.061.0005. | Organic Syntheses | |
| ALKENES via HOFMANN ELIMINATION: USE OF ION-EXCHANGE RESIN FOR PREPARATION OF QUATERNARY AMMONIUM HYDROXIDES: DIPHENYLMETHYL VINYL ETHER (Benzene, 1,1'-[(ethenyloxy)methylene]bis-) Rearrangement | Preparation of Benzene, 1,1'-[(ethenyloxy)methylene]bis-. Submitted by Carl Kaiser and Joseph Weinstock1. DOI: 10.15227/orgsyn.055.0003. | Organic Syntheses | |
| ALKOXYCARBONYLATION OF PROPARGYL CHLORIDE: METHYL 4-CHLORO-2-BUTYNOATE (2-Butynoic acid, 4-chloro-, methyl ester) | Preparation of 2-Butynoic acid, 4-chloro-, methyl ester. Submitted by M. Olomucki and J. Y. Le Gall1. DOI: 10.15227/orgsyn.065.0047. | Organic Syntheses | |
| ALKYL AND ALKYLENE BROMIDES (I. HYDROBROMIC ACID METHOD) | Preparation of I. HYDROBROMIC ACID METHOD. Submitted by Oliver Kamm and C. S. Marvel. DOI: 10.15227/orgsyn.001.0003. | Organic Syntheses | |
| ALKYLATION OF DIMEDONE WITH A TRICARBONYL(DIENE)IRON COMPLEX: TRICARBONYL[2-[(2,3,4,5-η)-4-METHOXY-2,4-CYCLOHEXADIEN-1-YL]-5,5-DIMETHYL-1,3-CYCLOHEXANEDIONE]IRON (Iron, tricarbonyl[2-[(2,3,4,5-η)-4-methoxy-2,4-cyclohexadien-1-yl]-5,5-dimethyl-1,3-cyclohexanedione]-) | Preparation of Iron, tricarbonyl[2-[(2,3,4,5-η)-4-methoxy-2,4-cyclohexadien-1-yl]-5,5-dimethyl-1,3-cyclohexanedione]-. Submitted by A. J. Birch and K. B. Chamberlain1. DOI: 10.15227/orgsyn.057.0016. | Organic Syntheses | |
| ALKYLATION OF ISOQUINOLINES via 2-BENZOYL-1,2-DIHYDROISOQUINALDONITRILES: 1-BENZYLISOQUINOLINE (Isoquinoline, 1-(phenylmethyl)-) | Preparation of Isoquinoline, 1-(phenylmethyl)-. Submitted by Barrie C. Uff1, John R. Kershaw1, and John L. Neumeyer2. DOI: 10.15227/orgsyn.056.0019. | Organic Syntheses | |
| ALKYLATION OF THE ANION FROM BIRCH REDUCTION OF o-ANISIC ACID: 2-HEPTYL-2-CYCLOHEXENONE Reduction | Preparation of ALKYLATION OF THE ANION FROM BIRCH REDUCTION OF o-ANISIC ACID: 2-HEPTYL-2-CYCLOHEXENONE. Submitted by D. F. Taber, B. P. Gunn, and I-Ching Chiu1. DOI: 10.15227/orgsyn.061.0059. | Organic Syntheses | |
| ALKYLATIONS OF ALDEHYDES via REACTION OF THE MAGNESIOENAMINE SALT OF AN ALDEHYDE: 2,2-DIMETHYL-3-PHENYLPROPIONALDEHYDE (Benzenepropanal, α,α-dimethyl-) | Preparation of Benzenepropanal, α,α-dimethyl-. Submitted by G. Stork1 and S. R. Dowd2. DOI: 10.15227/orgsyn.054.0046. | Organic Syntheses | |
| ALKYLATIONS USING HEXACARBONYL(PROPARGYLIUM)DICOBALT SALTS: 2-(1-METHYL-2-PROPYNYL)CYCLOHEXANONE (Cyclohexanone, 2-(1-methyl-2-propynyl)-, (R*,R*) and (R*,S*)-) | Preparation of Cyclohexanone, 2-(1-methyl-2-propynyl)-, (R*,R*) and (R*,S*)-. Submitted by Valsamma Varghese, Manasi Saha, and Kenneth M. Nicholas1. DOI: 10.15227/orgsyn.067.0141. | Organic Syntheses | |
| ALKYLIDENATION OF ESTER CARBONYL GROUPS: (Z)-1-ETHOXY-1-PHENYL-1-HEXENE | Preparation of ALKYLIDENATION OF ESTER CARBONYL GROUPS: (Z)-1-ETHOXY-1-PHENYL-1-HEXENE. Submitted by Kazuhiko Takai1, Yasutaka Kataoka, Jiro Miyai, Takashi Okazoe, Koichiro Oshima, and Kiitiro Utimoto… | Organic Syntheses | |
| ALKYL IODIDES: NEOPENTYL IODIDE AND IODOCYCLOHEXANE (Propane, 1-iodo-2,2-dimethyl- and Cyclohexane, iodo-) | Preparation of Propane, 1-iodo-2,2-dimethyl- and Cyclohexane, iodo-. Submitted by H. N. Rydon1. DOI: 10.15227/orgsyn.051.0044. | Organic Syntheses | |
| ALKYNES via PHASE TRANSFER–CATALYZED DEHYDROHALOGENATION: PROPIOLALDEHYDE DIETHYL ACETAL (1-Propyne, 3,3-diethoxy-) Halogenation | Preparation of 1-Propyne, 3,3-diethoxy-. Submitted by A. Le Coq1 and A. Gorgues. DOI: 10.15227/orgsyn.059.0010. | Organic Syntheses | |
| ALKYNE via SOLID-LIQUID PHASE-TRANSFER CATALYZED DEHYDROHALOGENATION: ACETYLENE DICARBOXALDEHYDE TETRAMETHYL ACETAL AND ACETYLENE DICARBOXALDEHYDE DIMETHYL ACETAL (1,1,4,4-Tetramethoxy-2-butyne and 4,4-Dimethoxy-2-Butynal) Halogenation | Preparation of 1,1,4,4-Tetramethoxy-2-butyne and 4,4-Dimethoxy-2-Butynal. Submitted by Rufine Akué-Gédu and Benoît Rigo1. DOI: 10.15227/orgsyn.082.0179. | Organic Syntheses | |
| ALKYNYL(PHENYL)IODONIUM TOSYLATES: PREPARATION AND STEREOSPECIFIC COUPLING WITH VINYLCOPPER REAGENTS. FORMATION OF CONJUGATED ENYNES. 1-HEXYNYL(PHENYL)IODONIUM TOSYLATE AND (E)-5-PHENYLDODEC-5-EN-7-YNE (Iodine, 1-hexynyl(4-methylbenzenesulfonato-O)phenyl- and Benzene, (1-butyl-1-octen-3-ynyl)-, (E)-) Cross-coupling | Preparation of Iodine, 1-hexynyl(4-methylbenzenesulfonato-O)phenyl- and Benzene, (1-butyl-1-octen-3-ynyl)-, (E)-. Submitted by Peter J. Stang and Tsugio Kitamura1. DOI: 10.15227/orgsyn.070.0215. | Organic Syntheses | |
| Allan–Robinson reaction Cyclization | The Allan–Robinson reaction is the chemical reaction of o-hydroxyaryl ketones with aromatic anhydrides to form flavones (or isoflavones). | Wikipedia: Category:Name reactions | |
| ALLANTOIN | Preparation of ALLANTOIN. Submitted by W. W. Hartman, E. W. Moffett, and J. B. Dickey. DOI: 10.15227/orgsyn.013.0001. | Organic Syntheses | |
| ALLENE | Preparation of ALLENE. Submitted by H. N. Cripps1 and E. F. Kiefer2. DOI: 10.15227/orgsyn.042.0012. | Organic Syntheses | |
| Allen–Millar–Trippett rearrangement Rearrangement | The Allen–Millar–Trippett rearrangement is a ring expansion reaction in which a cyclic phosphine is transformed into a cyclic phosphine oxide. This name reaction, first reported in the 1960s by David … | Wikipedia: Category:Name reactions | |
| ALLOXAN MONOHYDRATE (Alloxan) | Preparation of Alloxan. Submitted by W. W. Hartman and O. E. Sheppard. DOI: 10.15227/orgsyn.023.0003. | Organic Syntheses | |
| ALLOXAN MONOHYDRATE (Barbituric acid, 5,5-dihydroxy-) | Preparation of Barbituric acid, 5,5-dihydroxy-. Submitted by A. V. Holmgren and Wilhelm Wenner1. DOI: 10.15227/orgsyn.032.0006. | Organic Syntheses | |
| ALLOXANTIN DIHYDRATE | Preparation of ALLOXANTIN DIHYDRATE. Submitted by R. Stuart Tipson1. DOI: 10.15227/orgsyn.033.0003. | Organic Syntheses | |
| ALLOXANTIN DIHYDRATE | Preparation of ALLOXANTIN DIHYDRATE. Submitted by Dorothy Nightingale. DOI: 10.15227/orgsyn.023.0006. | Organic Syntheses | |
| ALLYL ALCOHOL | Preparation of ALLYL ALCOHOL. Submitted by Oliver Kamm and C. S. Marvel. DOI: 10.15227/orgsyn.001.0015. | Organic Syntheses | |
| ALLYLAMINE | Preparation of ALLYLAMINE. Submitted by M. T. Leffler. DOI: 10.15227/orgsyn.018.0005. | Organic Syntheses | |
| ALLYLBORONATION OF IMINES: 1-PHENYLHEX-5-EN-3-AMINE | Preparation of ALLYLBORONATION OF IMINES: 1-PHENYLHEX-5-EN-3-AMINE. Submitted by Masaharu Sugiura, Keiichi Hirano, and Shu¯ Kobayashi1. DOI: 10.15227/orgsyn.083.0170. | Organic Syntheses | |
| ALLYLCARBAMATES BY THE AZA-ENE REACTION: METHYL N-(2-METHYL-2-BUTENYL)CARBAMATE (Carbamic acid, (2-methyl-2-butenyl)-, methyl ester) | Preparation of Carbamic acid, (2-methyl-2-butenyl)-, methyl ester. Submitted by Günter Kresze, Hans Braxmeier, and Heribert Münsterer1. DOI: 10.15227/orgsyn.065.0159. | Organic Syntheses | |
| Allyl Cyanate-To-Isocyanate Rearrangement: Preparation of tert-Butyl 3,7-dimethylocta-1,6-dien-3-ylcarbamate Rearrangement | Preparation of Allyl Cyanate-To-Isocyanate Rearrangement: Preparation of tert-Butyl 3,7-dimethylocta-1,6-dien-3-ylcarbamate. Submitted by Yoshiyasu Ichikawa,1 Noriko Kariya, and Tomoyuki Hasegawa. DOI… | Organic Syntheses | |
| ALLYL CYANIDE (3-Butenenitrile) | Preparation of 3-Butenenitrile. Submitted by J. V. Supniewski and P. L. Salzberg. DOI: 10.15227/orgsyn.008.0004. | Organic Syntheses | |
| ALLYLIC ACETOXYLATION OF CYCLOALKENES: 2-CYCLOHEPTEN-1-YL ACETATE (2-Cyclohepten-1-ol, acetate) | Preparation of 2-Cyclohepten-1-ol, acetate. Submitted by A. Heumann1, B. Åkermark2, S. Hansson2, and T. Rein2. DOI: 10.15227/orgsyn.068.0109. | Organic Syntheses | |
| ALLYLIC ALCOHOLS BY ALKENE TRANSFER FROM ZIRCONIUM TO ZINC: 1-[(tert-BUTYLDIPHENYLSILYL)OXY]-DEC-3-EN-5-OL | Preparation of ALLYLIC ALCOHOLS BY ALKENE TRANSFER FROM ZIRCONIUM TO ZINC: 1-[(tert-BUTYLDIPHENYLSILYL)OXY]-DEC-3-EN-5-OL. Submitted by Peter Wipf and Wenjing Xu1. DOI: 10.15227/orgsyn.074.0205. | Organic Syntheses | |
| ALLYLICALLY TRANSPOSED AMINES FROM ALLYLIC ALCOHOLS: 3,7-DIMETHYL-1,6-OCTADIEN-3-AMINE (1,6-Octadien-3-amine, 3,7-dimethyl-) | Preparation of 1,6-Octadien-3-amine, 3,7-dimethyl-. Submitted by Lane A. Clizbe and Larry E. Overman1. DOI: 10.15227/orgsyn.058.0004. | Organic Syntheses | |
| ALLYLIC CHLORIDES FROM ALLYLIC ALCOHOLS: GERANYL CHLORIDE (2,6-Octadiene, 1-chloro-3,7-dimethyl-, (E)-) | Preparation of 2,6-Octadiene, 1-chloro-3,7-dimethyl-, (E)-. Submitted by Gilbert Stork1, Paul A. Grieco2, and Michael Gregson. DOI: 10.15227/orgsyn.054.0068. | Organic Syntheses | |
| Allylic Oxidation Catalyzed by Dirhodium(II) Tetrakis[ε-caprolactamate] of tert-Butyldimethylsilyl-protected trans-Dehydroandrosterone Oxidation | Preparation of Allylic Oxidation Catalyzed by Dirhodium(II) Tetrakis[ε-caprolactamate] of tert-Butyldimethylsilyl-protected trans-Dehydroandrosterone. Submitted by Maxim O. Ratnikov1*, Petra L. Goldma… | Organic Syntheses | |
| ALLYLIC OXIDATION WITH HYDROGEN PEROXIDE–SELENIUM DIOXIDE: trans-PINOCARVEOL (Bicyclo[3.1.1]heptan-3-ol, 6,6-dimethyl-2-methylene-, (1α,3α,5α)-) Oxidation | Preparation of Bicyclo[3.1.1]heptan-3-ol, 6,6-dimethyl-2-methylene-, (1α,3α,5α)-. Submitted by J. M. Coxon, E. Dansted, and M. P. Hartshorn1. DOI: 10.15227/orgsyn.056.0025. | Organic Syntheses | |
| ALLYLINDATION IN AQUEOUS MEDIA: METHYL 3-(HYDROXYMETHYL)-4-METHYL-2-METHYLENEPENTANOATE | Preparation of ALLYLINDATION IN AQUEOUS MEDIA: METHYL 3-(HYDROXYMETHYL)-4-METHYL-2-METHYLENEPENTANOATE. Submitted by George D. Bennett and Leo A. Paquette1. DOI: 10.15227/orgsyn.077.0107. | Organic Syntheses | |
| ALLYL LACTATE (Lactic acid, allyl ester) | Preparation of Lactic acid, allyl ester. Submitted by Chessie E. Rehberg. DOI: 10.15227/orgsyn.026.0004. | Organic Syntheses | |
| ALLYLTRIBUTYLTIN (Stannane, tributyl-2-propenyl-) | Preparation of Stannane, tributyl-2-propenyl-. Submitted by Noreen G. Halligan and Larry C. Blaszczak1. DOI: 10.15227/orgsyn.068.0104. | Organic Syntheses | |
| ALUMINUM tert-BUTOXIDE | Preparation of ALUMINUM tert-BUTOXIDE. Submitted by Winston Wayne and Homer Adkins. DOI: 10.15227/orgsyn.021.0008. | Organic Syntheses | |
| Amadori rearrangement Rearrangement | The Amadori rearrangement is an organic reaction describing the acid or base catalyzed isomerization or rearrangement reaction of the N-glycoside of an aldose or the glycosylamine to the corresponding… | Wikipedia: Category:Name reactions |
