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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 |
|---|---|---|---|
| ACETONE DIBUTYL ACETAL (Propane, 2,2-dibutoxy-) | Preparation of Propane, 2,2-dibutoxy-. Submitted by N. B. Lorette and W. L. Howard1. DOI: 10.15227/orgsyn.042.0001. | Organic Syntheses | |
| ACETONEDICARBOXYLIC ACID (Glutaric acid, β-oxo) | Preparation of Glutaric acid, β-oxo. Submitted by Roger Adams, H. M. Chiles, and C. F. Rassweiler. DOI: 10.15227/orgsyn.005.0005. | Organic Syntheses | |
| ACETONE HYDRAZONE (2-Propanone, hydrazone) | Preparation of 2-Propanone, hydrazone. Submitted by A. C. Day1 and M. C. Whiting2. DOI: 10.15227/orgsyn.050.0003. | Organic Syntheses | |
| ACETONE TRIMETHYSILYL ENOL ETHER (Silane trimethyl[(1-methylethenyl)oxy]-) | Preparation of Silane trimethyl[(1-methylethenyl)oxy]-. Submitted by Nigel D. A. Walshe, Graham B. T. Goodwin, Graham C. Smith, and Frank E. Woodward1. DOI: 10.15227/orgsyn.065.0001. | Organic Syntheses | |
| ACETO-p-CYMENE (Acetophenone, 5-isopropyl-2-methyl-) | Preparation of Acetophenone, 5-isopropyl-2-methyl-. Submitted by C. F. H. Allen. DOI: 10.15227/orgsyn.014.0001. | Organic Syntheses | |
| ACETYLACETONE (Diacetylmethane; 2,4-pentanedione) | Preparation of Diacetylmethane; 2,4-pentanedione. Submitted by C. E. Denoon, Jr. DOI: 10.15227/orgsyn.020.0006. | Organic Syntheses | |
| ACETYLBENZOYL (1,2-Propanedione, 1-phenyl-) | Preparation of 1,2-Propanedione, 1-phenyl-. Submitted by W. W. Hartman and L. J. Roll. DOI: 10.15227/orgsyn.023.0001. | Organic Syntheses | |
| ACETYLENEDICARBOXYLIC ACID | Preparation of ACETYLENEDICARBOXYLIC ACID. Submitted by T. W. Abbott, Richard T. Arnold, and Ralph B. Thompson. DOI: 10.15227/orgsyn.018.0003. | Organic Syntheses | |
| ACETYLENIC ETHERS FROM ALCOHOLS AND THEIR REDUCTION TO Z- AND E-ENOL ETHERS: PREPARATION OF 1-MENTHOXY-1-BUTYNE FROM MENTHOL AND CONVERSION TO (Z)- AND (E)-1-MENTHOXY-1-BUTENE ([Cyclohexane, 2-(1-butynyloxy)-4-methyl-1-(1-methylethyl)-[1S-(1α,2β,4β)]-], and [[[Cyclohexane, 2-(1-butenyloxy)-4-methyl-1-(1-methylethyl)-, [1S-[1α,2β(Z),4β]]- and [1S-[1α,2β(E),4β]]-) Reduction | Preparation of [Cyclohexane, 2-(1-butynyloxy)-4-methyl-1-(1-methylethyl)-[1S-(1α,2β,4β)]-], and [[[Cyclohexane, 2-(1-butenyloxy)-4-methyl-1-(1-methylethyl)-, [1S-[1α,2β(Z),4β]]- and [1S-[1α,2β(E),4β]]… | Organic Syntheses | |
| ACETYLGLYCINE (Aceturic acid) | Preparation of Aceturic acid. Submitted by R. M. Herbst and D. Shemin. DOI: 10.15227/orgsyn.019.0004. | Organic Syntheses | |
| ACETYLMANDELIC ACID and ACETYLMANDELYL CHLORIDE ((Mandelic acid, acetate) (Mandelyl chloride, acetate)) | Preparation of (Mandelic acid, acetate) (Mandelyl chloride, acetate). Submitted by F. K. Thayer. DOI: 10.15227/orgsyn.004.0001. | Organic Syntheses | |
| ACETYLTRIMETHYLSILANE (Silane, acetyltrimethyl-) | Preparation of Silane, acetyltrimethyl-. Submitted by John A. Soderquist1. DOI: 10.15227/orgsyn.068.0025. | Organic Syntheses | |
| Achmatowicz reaction | The Achmatowicz reaction, also known as the Achmatowicz rearrangement or the Achmatowicz oxidation, is an organic synthesis in which a furan is converted to a dihydropyran. In the original publication… | Wikipedia: Category:Name reactions | |
| ACID AMMONIUM o-SULFOBENZOATE (Benzoic acid, o-sulfo-, ammonium H salt) | Preparation of Benzoic acid, o-sulfo-, ammonium H salt. Submitted by H. T. Clarke and E. E. Dreger. DOI: 10.15227/orgsyn.009.0001. | Organic Syntheses | |
| ACID ANHYDRIDES | Preparation of ACID ANHYDRIDES. Submitted by C. F. H. Allen, C. J. Kibler, D. M. McLachlin, and C. V. Wilson. DOI: 10.15227/orgsyn.026.0001. | Organic Syntheses | |
| ACID CHLORIDES FROM α-KETO ACIDS WITH α,α-DICHLOROMETHYL METHYL ETHER: PYRUVOYL CHLORIDE (Propanoyl chloride, 2-oxo-) | Preparation of Propanoyl chloride, 2-oxo-. Submitted by Harry C. J. Ottenheijm and Marianne W. Tijhuis1. DOI: 10.15227/orgsyn.061.0001. | Organic Syntheses | |
| ACONITIC ACID | Preparation of ACONITIC ACID. Submitted by William F. Bruce. DOI: 10.15227/orgsyn.017.0001. | Organic Syntheses | |
| A CONVENIENT PREPARATION OF AN ORTHOGONALLY PROTECTED Cα,Cα-DISUBSTITUTED AMINO ACID ANALOG OF LYSINE: 1-tert-BUTYLOXYCARBONYL-4-((9-FLUORENYLMETHYLOXYCARBONYL)AMINO)-PIPERIDINE-4-CARBOXYLIC ACID ([1,4-Piperidinedicarboxylic acid, 4-[[(9H-fluoren-9-ylmethyloxy)carbonyl]amino]-, (1,1-dimethylethyl) ester]) | Preparation of [1,4-Piperidinedicarboxylic acid, 4-[[(9H-fluoren-9-ylmethyloxy)carbonyl]amino]-, (1,1-dimethylethyl) ester]. Submitted by Lars G. J. Hammarström, Yanwen Fu, Sidney Vail, Robert P. Hamm… | Organic Syntheses | |
| ACRIDONE | Preparation of ACRIDONE. Submitted by C. F. H. Allen and G. H. W. McKee. DOI: 10.15227/orgsyn.019.0006. | Organic Syntheses | |
| ACROLEIN | Preparation of ACROLEIN. Submitted by Homer Adkins and W. H. Hartung. DOI: 10.15227/orgsyn.006.0001. | Organic Syntheses | |
| ACROLEIN ACETAL (Acrolein diethyl acetal) | Preparation of Acrolein diethyl acetal. Submitted by J. A. VanAllan1. DOI: 10.15227/orgsyn.032.0005. | Organic Syntheses | |
| ACROLEIN ACETAL (Acrolein, diethyl acetal) | Preparation of Acrolein, diethyl acetal. Submitted by E. J. Witzemann, Wm. Lloyd Evans, Henry Hass, and E. F. Schroeder. DOI: 10.15227/orgsyn.011.0001. | Organic Syntheses | |
| ACRYLIC ACID (I. PYROLYSIS METHOD) | Preparation of I. PYROLYSIS METHOD. Submitted by W. P. Ratchford. DOI: 10.15227/orgsyn.029.0002. | Organic Syntheses | |
| ac-TETRAHYDRO-β-NAPHTHYLAMINE (2-Naphthylamine, 1,2,3,4-tetrahydro-) | Preparation of 2-Naphthylamine, 1,2,3,4-tetrahydro-. Submitted by E. B. H. Waser and H. Möllering. DOI: 10.15227/orgsyn.009.0084. | Organic Syntheses | |
| ACYLAMIDOALKYL ACETOPHENONES FROM SUBSTITUTED PHENETHYLAMINES: 2-(2-ACETAMIDOETHYL)-4,5-DIMETHOXYACETOPHENONE (Acetamide, N-[2-(2-acetyl-4,5-dimethoxyphenyl)ethyl]-) | Preparation of Acetamide, N-[2-(2-acetyl-4,5-dimethoxyphenyl)ethyl]-. Submitted by A. Brossi, L. A. Dolan, and S. Teitel1. DOI: 10.15227/orgsyn.056.0003. | Organic Syntheses | |
| ACYLOIN CONDENSATION BY THIAZOLIUM ION CATALYSIS: BUTYROIN (4-Octanone, 5-hydroxy-) Condensation | Preparation of 4-Octanone, 5-hydroxy-. Submitted by H. Stetter and H. Kuhlmann1. DOI: 10.15227/orgsyn.062.0170. | Organic Syntheses | |
| ACYLOIN CONDENSATION IN WHICH CHLOROTRIMETHYLSILANE IS USED AS A TRAPPING AGENT: 1,2-BIS(TRIMETHYLSILYLOXY)CYCLOBUTENE AND 2-HYDROXYCYCLOBUTANONE (Trimethylsilane, 1-cyclobuten-1,2-ylenedioxybis- and Cyclobutanone, 2-hydroxy-) Condensation | Preparation of Trimethylsilane, 1-cyclobuten-1,2-ylenedioxybis- and Cyclobutanone, 2-hydroxy-. Submitted by Jordan J. Bloomfield1 and Janice M. Nelke. DOI: 10.15227/orgsyn.057.0001. | Organic Syntheses | |
| ADAMANTANE (Tricyclo[3.3.1.13,7] decane) | Preparation of Tricyclo[3.3.1.13,7] decane. Submitted by Paul von R. Schleyer, M. M. Donaldson, R. D. Nicholas, and C. Cupas1. DOI: 10.15227/orgsyn.042.0008. | Organic Syntheses | |
| ADAMANTANONE (Tricyclo[3.3.1.13,7]decanone) | Preparation of Tricyclo[3.3.1.13,7]decanone. Submitted by H. W. Geluk and V. G. Keizer1. DOI: 10.15227/orgsyn.053.0008. | Organic Syntheses | |
| Adams decarboxylation | The Adams decarboxylation is a chemical reaction that involved the decarboxylation of coumarins which have carboxylic acid group in the third position. The decarboxylation is achieved by aqueous solut… | Wikipedia: Category:Name reactions | |
| ADDITION OF AN ETHYLCOPPER COMPLEX TO 1-OCTYNE: (E)-5-ETHYL-1,4-UNDECADIENE (1,4-Undecadiene, 5-ethyl-, (E)-) Addition | Preparation of 1,4-Undecadiene, 5-ethyl-, (E)-. Submitted by Ramnath S. Iyer and Paul Helquist1. DOI: 10.15227/orgsyn.064.0001. | Organic Syntheses | |
| ADDITION OF DIALKYLAMINES TO MYRCENE: N,N-DIETHYLGERANYLAMINE (2,6-Octadien-1-amine, N,N-diethyl-3,7-dimethyl-, (E)-) Addition | Preparation of 2,6-Octadien-1-amine, N,N-diethyl-3,7-dimethyl-, (E)-. Submitted by Kunihiko Takabe1, Takao Katagiri1, Juntaro Tanaka1, Tsutomu Fujita2, Shoji Watanabe2, and Kyoichi Suga2. DOI: 10.1522… | Organic Syntheses | |
| ADDITION OF ORGANOLITHIUM REAGENTS TO ALLYL ALCOHOL: 2-METHYL-1-HEXANOL (1-Hexanol, 2-methyl-) Addition | Preparation of 1-Hexanol, 2-methyl-. Submitted by J. K. Crandall1 and A. C. Rojas. DOI: 10.15227/orgsyn.055.0001. | Organic Syntheses | |
| ADIPIC ACID | Preparation of ADIPIC ACID. Submitted by B. A. Ellis. DOI: 10.15227/orgsyn.005.0009. | Organic Syntheses | |
| Adkins–Peterson reaction | The Adkins–Peterson reaction is the air oxidation of methanol to formaldehyde with metal oxide catalysts such as iron oxide, molybdenum trioxide or combinations thereof. | Wikipedia: Category:Name reactions | |
| A GENERAL [3+2] ANNULATION: cis-4-exo-ISOPROPENYL-1,9-DIMETHYL-8-(TRIMETHYLSILYL)BICYCLO[4.3.0]NON-8-EN-2-ONE (4H-Inden-4-one, 1,3a,5,6,7,7a-hexahydro-3,3a-dimethyl-6-(1-methylethenyl)-2-(trimethylsilyl)-, (3aα,6α,7aα)-) Cyclization | Preparation of 4H-Inden-4-one, 1,3a,5,6,7,7a-hexahydro-3,3a-dimethyl-6-(1-methylethenyl)-2-(trimethylsilyl)-, (3aα,6α,7aα)-. Submitted by Rick L. Danheiser, David M. Fink, and Yeun-Min Tsai1. DOI: 10.… | Organic Syntheses | |
| A GENERAL METHOD FOR COPPER-CATALYZED ARYLATION OF ACIDIC ARENE C-H BONDS. PREPARATION OF 2-CHLORO-5-(3-METHYLPHENYL)-THIOPHENE | Preparation of A GENERAL METHOD FOR COPPER-CATALYZED ARYLATION OF ACIDIC ARENE C-H BONDS. PREPARATION OF 2-CHLORO-5-(3-METHYLPHENYL)-THIOPHENE. Submitted by Joseph Alvarado, Hien-Quang Do, and Olafs D… | Organic Syntheses | |
| A GENERAL METHOD FOR THE PREPARATION OF 9-, 10-, AND 11-MEMBERED UNSATURATED MACROLIDES: SYNTHESIS OF 8-PROPIONYL-(E)-5-NONENOLIDE (2H-Oxecin-2-one, 3,4,5,8,9,10-hexahydro-9-(1-oxopropyl)-, (E)-) | Preparation of 2H-Oxecin-2-one, 3,4,5,8,9,10-hexahydro-9-(1-oxopropyl)-, (E)-. Submitted by Kevin S. Webb, Edward Asirvatham, and Gary H. Posner1. DOI: 10.15227/orgsyn.069.0188. | Organic Syntheses | |
| A GENERAL METHOD FOR THE SYNTHESIS OF ALLENYLSILANES: 1-METHYL-1-(TRIMETHYLSILYL)ALLENE (Silane, trimethyl(1-methyl-1,2-propadienyl)-) | Preparation of Silane, trimethyl(1-methyl-1,2-propadienyl)-. Submitted by Rick L. Danheiser, Yeun-Min Tsai, and David M. Fink1. DOI: 10.15227/orgsyn.066.0001. | Organic Syntheses | |
| A GENERAL PROCEDURE FOR MITSUNOBU INVERSION OF STERICALLY HINDERED ALCOHOLS: INVERSION OF MENTHOL. (1S,2S,5R)-5-METHYL-2-(1-METHYLETHYL)CYCLOHEXYL 4-NITROBENZOATE (Cyclohexanol, 5-methyl-2-(1-methylethyl)-, 4-nitrobenzoate, [1S-(1α,2α,5β)]-) Substitution | Preparation of Cyclohexanol, 5-methyl-2-(1-methylethyl)-, 4-nitrobenzoate, [1S-(1α,2α,5β)]-. Submitted by Jeffrey A. Dodge, Jeffrey S. Nissen, and Misti Presnell1. DOI: 10.15227/orgsyn.073.0110. | Organic Syntheses | |
| A GENERAL SYNTHESIS OF 4-ISOXAZOLECARBOXYLIC ESTERS: ETHYL 3-ETHYL-5-METHYL-4-ISOXAZOLECARBOXYLATE (4-Isoxazolecarboxylic acid, 3-ethyl-5-methyl-, ethyl ester) | Preparation of 4-Isoxazolecarboxylic acid, 3-ethyl-5-methyl-, ethyl ester. Submitted by John E. McMurry1. DOI: 10.15227/orgsyn.053.0059. | Organic Syntheses | |
| A GENERAL SYNTHESIS OF CYCLOBUTANONES FROM OLEFINS AND TERTIARY AMIDES: 3-HEXYLCYCLOBUTANONE | Preparation of A GENERAL SYNTHESIS OF CYCLOBUTANONES FROM OLEFINS AND TERTIARY AMIDES: 3-HEXYLCYCLOBUTANONE. Submitted by C. Schmit, J. B. Falmagne, J. Escudero, H. Vanlierde, and L. Ghosez1. DOI: 10.… | Organic Syntheses | |
| A GENERAL SYNTHETIC METHOD FOR THE OXIDATION OF PRIMARY ALCOHOLS TO ALDEHYDES: (S)-(+)-2-METHYLBUTANAL (Butanal, 2-methyl-, (S)-) Oxidation | Preparation of Butanal, 2-methyl-, (S)-. Submitted by Pier Lucio Anelli, Fernando Montanari, and Silvio Quici1. DOI: 10.15227/orgsyn.069.0212. | Organic Syntheses | |
| A GENERAL SYNTHETIC METHOD FOR THE PREPARATION OF CONJUGATED DIENES FROM OLEFINS USING BROMOMETHANESULFONYL BROMIDE: 1,2-DIMETHYLENECYCLOHEXANE (Cyclohexane, 1,2-bis(methylene)-) | Preparation of Cyclohexane, 1,2-bis(methylene)-. Submitted by Eric Block and Mohammad Aslam1. DOI: 10.15227/orgsyn.065.0090. | Organic Syntheses | |
| A GENERAL SYNTHETIC METHOD FOR THE PREPARATION OF METHYL KETONES FROM TERMINAL OLEFINS: 2-DECANONE | Preparation of A GENERAL SYNTHETIC METHOD FOR THE PREPARATION OF METHYL KETONES FROM TERMINAL OLEFINS: 2-DECANONE. Submitted by Jiro Tsuji, Hideo Nagashima, and Hisao Nemoto1. DOI: 10.15227/orgsyn.062… | Organic Syntheses | |
| A HYDROXYMETHYL ANION EQUIVALENT: TRIBUTYL[(METHOXYMETHOXY)METHYL]STANNANE (Stannane, tributyl[(methoxymethoxy)methyl]-) | Preparation of Stannane, tributyl[(methoxymethoxy)methyl]-. Submitted by Rick L. Danheiser1, Karen R. Romines1, Hiroo Koyama1, Stephen K. Gee1, Carl R. Johnson2, and John R. Medich2. DOI: 10.15227/org… | Organic Syntheses | |
| Air Oxidation of Primary Alcohols Catalyzed by Copper(I)/TEMPO. Preparation of 2-Amino-5-bromobenzaldehyde Oxidation | Preparation of Air Oxidation of Primary Alcohols Catalyzed by Copper(I)/TEMPO. Preparation of 2-Amino-5-bromobenzaldehyde. Submitted by Jessica M. Hoover and Shannon S. Stahl. 1. DOI: 10.15227/orgsyn.… | Organic Syntheses | |
| Akabori amino-acid reaction | There are several Akabori amino acid reactions, which are named after Shirō Akabori (Japanese: 赤堀 四郎) (1900–1992), a Japanese chemist. | Wikipedia: Category:Name reactions | |
| Albright–Goldman oxidation Oxidation | The Albright–Goldman oxidation is a name reaction of organic chemistry, first described by the American chemists J. Donald Albright and Leon Goldman in 1965. The reaction is particularly suitable for … | Wikipedia: Category:Name reactions | |
| ALDEHYDES BY OXIDATION OF TERMINAL OLEFINS WITH CHROMYL CHLORIDE: 2,4,4-TRIMETHYLPENTANAL (Pentanal, 2,4,4-trimethyl-) Oxidation | Preparation of Pentanal, 2,4,4-trimethyl-. Submitted by Fillmore Freeman1, Richard H. DuBois, and Thomas G. McLaughlin. DOI: 10.15227/orgsyn.051.0004. | Organic Syntheses |
