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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 |
|---|---|---|---|
| cis-STILBENE | Preparation of cis-STILBENE. Submitted by Robert E. Buckles and Norris G. Wheeler1. DOI: 10.15227/orgsyn.033.0088. | Organic Syntheses | |
| cis-α,β-UNSATURATED ACIDS: ISOCROTONIC ACID (2-Butenoic acid, (Z)-) | Preparation of 2-Butenoic acid, (Z)-. Submitted by C. Rappe1. DOI: 10.15227/orgsyn.053.0123. | Organic Syntheses | |
| cis-Δ4-TETRAHYDROPHTHALIC ANHYDRIDE (4-Cyclohexene-1,2-dicarboxylic anhydride, cis-) | Preparation of 4-Cyclohexene-1,2-dicarboxylic anhydride, cis-. Submitted by Arthur C. Cope and Elbert C. Herrick1. DOI: 10.15227/orgsyn.030.0093. | Organic Syntheses | |
| CITRACONIC ANHYDRIDE AND CITRACONIC ACID | Preparation of CITRACONIC ANHYDRIDE AND CITRACONIC ACID. Submitted by R. L. Shriner, S. G. Ford, and L. J. Roll. DOI: 10.15227/orgsyn.011.0028. | Organic Syntheses | |
| Claisen condensation Rearrangement | The Claisen condensation is a carbon–carbon bond forming reaction that occurs between two esters or one ester and another carbonyl compound in the presence of a strong base. The reaction produces a β… | Wikipedia: Category:Name reactions | |
| Claisen rearrangement Rearrangement | The Claisen rearrangement is a carbon–carbon bond-forming chemical reaction discovered by Rainer Ludwig Claisen. The heating of an allyl vinyl ether will initiate a [3,3]-sigmatropic rearrangement to … | Wikipedia: Category:Name reactions | |
| Claisen-Schmidt aldol: benzaldehyde + acetone → benzalacetone Scale Condensation | Textbook aldol condensation. Acetone's α-carbon (deprotonated by aqueous NaOH) attacks benzaldehyde, then β-elimination dehydrates the aldol intermediate to give the E-enone benzalacetone (4-phenyl-3-… | Claisen-Schmidt 1881 | |
| CLEAVAGE OF METHYL ETHERS WITH IODOTRIMETHYLSILANE: CYCLOHEXANOL FROM CYCLOHEXYL METHYL ETHER | Preparation of CLEAVAGE OF METHYL ETHERS WITH IODOTRIMETHYLSILANE: CYCLOHEXANOL FROM CYCLOHEXYL METHYL ETHER. Submitted by Michael E. Jung1 and Mark A. Lyster12. DOI: 10.15227/orgsyn.059.0035. | Organic Syntheses | |
| Clemmensen reduction Reduction | Clemmensen reduction is a chemical reaction described as a reduction of ketones or aldehydes to alkanes using zinc amalgam and concentrated hydrochloric acid (HCl). This reaction is named after Erik C… | Wikipedia: Category:Name reactions | |
| Collins oxidation Oxidation | The Collins oxidation is an organic reaction for the oxidation of primary alcohols to aldehydes. It is distinguished from other chromium oxide-based oxidations by the use of Collins reagent, a comple… | Wikipedia: Category:Name reactions | |
| Combes quinoline synthesis | The Combes quinoline synthesis is a chemical reaction, which was first reported by Combes in 1888. Further studies and reviews of the Combes quinoline synthesis and its variations have been published … | Wikipedia: Category:Name reactions | |
| CONDENSATION OF (−)-DIMENTHYL SUCCINATE DIANION WITH 1,ω-DIHALIDES: (+)-(1S,2S)-CYCLOPROPANE-1,2-DICARBOXYLIC ACID (1,2-Cyclopropanedicarboxylic acid, (1S,2S)-(+)-) Condensation | Preparation of 1,2-Cyclopropanedicarboxylic acid, (1S,2S)-(+)-. Submitted by Kyoji Furuta, Kiyoshi Iwanaga, and Hisashi Yamamoto1. DOI: 10.15227/orgsyn.067.0076. | Organic Syntheses | |
| CONDENSATION OF DIMETHYL 1,3-ACETONEDICARBOXYLATE WITH 1,2-DICARBONYL COMPOUNDS: cis-BICYCLO[3.3.0]OCTANE-3,7-DIONES (2,5(1H,3H)-Pentalenedione, tetrahydro-, cis-, and 2,5(1H,3H)-pentalenedione, tetrahydro-, 3a,6a-dimethyl-, cis) Condensation | Preparation of 2,5(1H,3H)-Pentalenedione, tetrahydro-, cis-, and 2,5(1H,3H)-pentalenedione, tetrahydro-, 3a,6a-dimethyl-, cis. Submitted by Steven H. Bertz1, James M. Cook2, Ali Gawish2, and Ulrich We… | Organic Syntheses | |
| CONJUGATE ADDITION–CYCLIZATION OF A CYANOCUPRATE: 2-CARBOMETHOXY-3-VINYLCYCLOPENTANONE (Cyclopentanecarboxylic acid, 2-ethenyl-5-oxo-, methyl ester) Cyclization | Preparation of Cyclopentanecarboxylic acid, 2-ethenyl-5-oxo-, methyl ester. Submitted by William A. Nugent and Frank W. Hobbs, Jr.1. DOI: 10.15227/orgsyn.066.0052. | Organic Syntheses | |
| CONJUGATE ADDITION OF A VINYLZIRCONIUM REAGENT: 3-(1-OCTEN-1-YL)CYCLOPENTANONE (Cyclopentanone, 3-(1-octenyl)-, (E)-) Addition | Preparation of Cyclopentanone, 3-(1-octenyl)-, (E)-. Submitted by Ruen Chu Sun1, Masami Okabe1, David L. Coffen1, and Jeffrey Schwartz2. DOI: 10.15227/orgsyn.071.0083. | Organic Syntheses | |
| CONJUGATE ALLYLATION OF α,β-UNSATURATED KETONES WITH ALLYLSILANES: 4-PHENYL-6-HEPTEN-2-ONE (6-Hepten-2-one, 4-phenyl-) | Preparation of 6-Hepten-2-one, 4-phenyl-. Submitted by Hideki Sakurai, Akira Hosomi, and Josabro Hayashi1. DOI: 10.15227/orgsyn.062.0086. | Organic Syntheses | |
| CONJUGATE REDUCTION OF α,β-UNSATURATED p-TOLUENESULFONYLHYDRAZONES TO ALKENES WITH CATECHOLBORANE: 5β-CHOLEST-3-ENE (Cholest-3-ene, (5β)-) Reduction | Preparation of Cholest-3-ene, (5β)-. Submitted by George W. Kabalka1, Robert Hutchins2, Nicholas R. Natale2, Dominic T. C. Yang3, and Vicky Broach3. DOI: 10.15227/orgsyn.059.0042. | Organic Syntheses | |
| Conrad–Limpach synthesis | The Conrad–Limpach synthesis is the condensation of anilines (1) with β-ketoesters (2) to form 4-hydroxyquinolines (4) via a Schiff base (3). The overall reaction type is a combination of both an addi… | Wikipedia: Category:Name reactions | |
| CONTROLLED-POTENTIAL ELECTROLYTIC REDUCTION: 1,1-BIS(BROMOMETHYL)CYCLOPROPANE (Cyclopropane, 1,1-bis(bromomethyl)-) Reduction | Preparation of Cyclopropane, 1,1-bis(bromomethyl)-. Submitted by M. R. Rifi1. DOI: 10.15227/orgsyn.052.0022. | Organic Syntheses | |
| CONVENIENT PREPARATION OF 3-ETHOXYCARBONYL BENZOFURANS FROM SALICYLALDEHYDES AND ETHYL DIAZOACETATE | Preparation of CONVENIENT PREPARATION OF 3-ETHOXYCARBONYL BENZOFURANS FROM SALICYLALDEHYDES AND ETHYL DIAZOACETATE. Submitted by Matthew E. Dudley, M. Monzur Morshed, and M. Mahmun Hossain1. DOI: 10.1… | Organic Syntheses | |
| Convenient Synthesis of α-Diazoacetates from α-Bromoacetates and N,N'-Ditosylhydrazine: Preparation of Benzyl Diazoacetate | Preparation of Convenient Synthesis of α-Diazoacetates from α-Bromoacetates and N,N'-Ditosylhydrazine: Preparation of Benzyl Diazoacetate. Submitted by Eiji Ideue, Tatsuya Toma, and Jun Shimokawa and … | Organic Syntheses | |
| CONVERSION OF AMINES TO PHOSPHO ESTERS: DECYL DIETHYL PHOSPHATE (Phosphoric acid, decyl diethyl ester) | Preparation of Phosphoric acid, decyl diethyl ester. Submitted by Nick Nikolaides, Ioanna Schipor, and Bruce Ganem1. DOI: 10.15227/orgsyn.072.0246. | Organic Syntheses | |
| CONVERSION OF ARYLALKYLKETONES INTO DICHLOROALKENES: (1-CHLORO-4-(2,2-DICHLORO-1-METHYLETHENYL)-BENZENE) (1-Chloro-4-(2,2-dichloro-1-methylethenyl)-benzene) | Preparation of 1-Chloro-4-(2,2-dichloro-1-methylethenyl)-benzene. Submitted by Valentine G. Nenajdenko1 , Vasily N. Korotchenko1, Alexey V. Shastin2, and Elisabeth S. Balenkova1. DOI: 10.15227/orgsyn.… | Organic Syntheses | |
| CONVERSION OF EPOXIDES TO β-HYDROXY ISOCYANIDES: trans-2-ISOCYANOCYCLOHEXANOL (Cyclohexanol, 2-isocyanato-, trans-) | Preparation of Cyclohexanol, 2-isocyanato-, trans-. Submitted by Paul G. Gassman and Thomas L. Guggenheim1. DOI: 10.15227/orgsyn.064.0039. | Organic Syntheses | |
| CONVERSION OF ESTERS TO ALLYLSILANES: TRIMETHYL(2-METHYLENE-4-PHENYL-3-BUTENYL)SILANE (Silane, trimethyl (2-methylene-4-phenyl-3-butenyl)-) | Preparation of Silane, trimethyl (2-methylene-4-phenyl-3-butenyl)-. Submitted by William H. Bunnelle and B. A. Narayanan1. DOI: 10.15227/orgsyn.069.0089. | Organic Syntheses | |
| CONVERSION OF ESTERS TO AMIDES WITH DIMETHYLALUMINUM AMIDES: N,N-DIMETHYLCYCLOHEXANECARBOXAMIDE | Preparation of CONVERSION OF ESTERS TO AMIDES WITH DIMETHYLALUMINUM AMIDES: N,N-DIMETHYLCYCLOHEXANECARBOXAMIDE. Submitted by Michael F. Lipton1, Anwer Basha1, and Steven M. Weinreb1,2. DOI: 10.15227/o… | Organic Syntheses | |
| CONVERSION OF KETONES TO CYANOHYDRINS: BENZOPHENONE CYANOHYDRIN (Benzeneacetonitrile, α-hydroxy-αphenyl) | Preparation of Benzeneacetonitrile, α-hydroxy-αphenyl. Submitted by Paul G. Gassman and John J. Talley1. DOI: 10.15227/orgsyn.060.0014. | Organic Syntheses | |
| CONVERSION OF METHYL KETONES INTO TERMINAL ACETYLENES: ETHYNYLFERROCENE (Ferrocene, ethynyl) | Preparation of Ferrocene, ethynyl. Submitted by Johann Polin and Herwig Schottenberger1. DOI: 10.15227/orgsyn.073.0262. | Organic Syntheses | |
| CONVERSION OF METHYL KETONES INTO TERMINAL ALKYNES: (E)-BUTEN-3-YNYL-2,6,6-TRIMETHYL-1-CYCLOHEXENE (Cyclohexene, 2-(1-buten-3-ynyl)-1,3,3-trimethyl-, (E)-) | Preparation of Cyclohexene, 2-(1-buten-3-ynyl)-1,3,3-trimethyl-, (E)-. Submitted by Ei-ichi Negishi, Anthony O. King, and James M. Tour1. DOI: 10.15227/orgsyn.064.0044. | Organic Syntheses | |
| CONVERSION OF NITRILES INTO TERTIARY AMINES: N,N-DIMETHYLHOMOVERATRYLAMINE (Benzeneethanamine, 3,4-dimethoxy-N,N-dimethyl-) | Preparation of Benzeneethanamine, 3,4-dimethoxy-N,N-dimethyl-. Submitted by Guilhem Rousselet1 , Patrice Capdevielle2 , and Michel Maumy2. DOI: 10.15227/orgsyn.076.0133. | Organic Syntheses | |
| CONVERSION OF NITRO TO CARBONYL BY OZONOLYSIS OF NITRONATES: 2,5-HEPTANEDIONE Oxidation | Preparation of CONVERSION OF NITRO TO CARBONYL BY OZONOLYSIS OF NITRONATES: 2,5-HEPTANEDIONE. Submitted by John E. McMurry1 and Jack Melton. DOI: 10.15227/orgsyn.056.0036. | Organic Syntheses | |
| CONVERSION OF PRIMARY ALCOHOLS TO URETHANES via THE INNER SALT OF METHYL (CARBOXYSULFAMOYL)TRIETHYLAMMONIUM HYDROXIDE: METHYL n-HEXYLCARBAMATE (Carbamic acid, hexyl-, methyl ester) | Preparation of Carbamic acid, hexyl-, methyl ester. Submitted by Edward M. Burgess1, Harold R. Penton, Jr., E. Alan Taylor, and W. Michael Williams. DOI: 10.15227/orgsyn.056.0040. | Organic Syntheses | |
| Cook–Heilbron thiazole synthesis | The Cook–Heilbron thiazole synthesis highlights the formation of 5-aminothiazoles through the chemical reaction of α-aminonitriles or aminocyanoacetates with dithioacids, carbon disulphide, carbon oxy… | Wikipedia: Category:Name reactions | |
| Cope reaction Rearrangement | The Cope reaction or Cope elimination, developed by Arthur C. Cope, is the elimination reaction of an N-oxide to an alkene and a hydroxylamine.Typically, the amine oxide is prepared from the correspon… | Wikipedia: Category:Name reactions | |
| Cope rearrangement Rearrangement | The Cope rearrangement (sometimes referred to as the Hardy–Cope rearrangement) is an extensively studied organic reaction involving the [3,3]-sigmatropic rearrangement of 1,5-dienes. It was developed … | Wikipedia: Category:Name reactions | |
| COPPER CATALYZED ARYLATION OF β-DICARBONYL COMPOUNDS: 2-(1-ACETYL-2-OXOPROPYL)BENZOIC ACID (Benzoic acid, 2-(1-acetyl-2-oxopropyl)-) | Preparation of Benzoic acid, 2-(1-acetyl-2-oxopropyl)-. Submitted by Alle Bruggink, Stephen J. Ray, and Alexander McKillop1. DOI: 10.15227/orgsyn.058.0052. | Organic Syntheses | |
| COPPER-CATALYZED CONJUGATE ADDITION OF A ZINC HOMOENOLATE: ETHYL 3-[3-(TRIMETHYLSILYLOXY)CYCLOHEX-2-ENYL]PROPIONATE (2-Cyclohexene-1-propanoic acid, 3-[(trimethylsilyl)oxy]-, ethyl ester) Addition | Preparation of 2-Cyclohexene-1-propanoic acid, 3-[(trimethylsilyl)oxy]-, ethyl ester. Submitted by Eiichi Nakamura and Isao Kuwajima1. DOI: 10.15227/orgsyn.066.0043. | Organic Syntheses | |
| COPPER-CATALYZED CONJUGATE ADDITION OF FUNCTIONALIZED ORGANOZINC REAGENTS TO α,β-UNSATURATED KETONES: ETHYL 5-(3-OXOCYCLOHEXYL)PENTANOATE (Pentanoic acid, 5-(3-oxocyclohexyl)-, ethyl ester) Addition | Preparation of Pentanoic acid, 5-(3-oxocyclohexyl)-, ethyl ester. Submitted by B. H. Lipshutz1 , M. R. Wood, and R. Tirado. DOI: 10.15227/orgsyn.076.0252. | Organic Syntheses | |
| COPPER-CATALYZED ELECTROPHILIC AMINATION OF DIORGANOZINC REAGENTS: 4-PHENYLMORPHOLINE | Preparation of COPPER-CATALYZED ELECTROPHILIC AMINATION OF DIORGANOZINC REAGENTS: 4-PHENYLMORPHOLINE. Submitted by Ashley M. Berman and Jeffrey S. Johnson1. DOI: 10.15227/orgsyn.083.0031. | Organic Syntheses | |
| COPPER-CATALYZED THREE-COMPONENT REACTION OF 1-ALKYNES, SULFONYL AZIDES, AND WATER: N-(4-ACETAMIDOPHENYLSULFONYL)-2-PHENYLACETAMIDE | Preparation of COPPER-CATALYZED THREE-COMPONENT REACTION OF 1-ALKYNES, SULFONYL AZIDES, AND WATER: N-(4-ACETAMIDOPHENYLSULFONYL)-2-PHENYLACETAMIDE. Submitted by Seung Hwan Cho, Seung Jun Hwang, and Su… | Organic Syntheses | |
| COPPER CHROMITE CATALYST | Preparation of COPPER CHROMITE CATALYST. Submitted by W. A. Lazier and H. R. Arnold. DOI: 10.15227/orgsyn.019.0031. | Organic Syntheses | |
| COPPER(I)-CATALYZED PHOTOCYCLOADDITION: 3,3-DIMETHYL-cis-BICYCLO[3.2.0]HEPTAN-2-ONE (Bicyclo[3.2.0]heptan-2-one, 3,3-dimethyl-) Cycloaddition | Preparation of Bicyclo[3.2.0]heptan-2-one, 3,3-dimethyl-. Submitted by Robert G. Salomon and Subrata Ghosh1. DOI: 10.15227/orgsyn.062.0125. | Organic Syntheses | |
| COPPER(I)-CATALYZED PREPARATION OF (E)-3-IODOPROP-2-ENOIC ACID ((2-Propenoic acid, 3-iodo-, (2E)-)) | Preparation of (2-Propenoic acid, 3-iodo-, (2E)-). Submitted by Darren J. Dixon, Steven V. Ley, and Deborah A. Longbottom1. DOI: 10.15227/orgsyn.080.0129. | Organic Syntheses | |
| COPPER(I) IODIDE DIMETHYL SULFIDE CATALYZED ADDITION OF A VINYLZIRCONIUM REAGENT (PREPARATION OF 4-PHENYL-5(E)-DECEN-2-ONE) Addition | Preparation of PREPARATION OF 4-PHENYL-5(E)-DECEN-2-ONE. Submitted by Amer El-Batta and Mikael Bergdahl1. DOI: 10.15227/orgsyn.084.0192. | Organic Syntheses | |
| Corey–Fuchs reaction | The Corey–Fuchs reaction, also known as the Ramirez–Corey–Fuchs reaction, is a series of chemical reactions designed to transform an aldehyde into an alkyne.[1][2][3] The formation of the 1,1-dibromo… | Wikipedia: Category:Name reactions | |
| Corey–House synthesis | The Corey–House synthesis (also called the Corey–Posner–Whitesides–House reaction and other permutations) is an organic reaction that involves the reaction of a lithium diorganylcuprate ( | Wikipedia: Category:Name reactions | |
| Corey–Itsuno reduction Reduction | The Corey–Itsuno reduction, also known as the Corey–Bakshi–Shibata (CBS) reduction, is a chemical reaction in which a prochiral ketone is enantioselectively reduced to produce the corresponding chiral… | Wikipedia: Category:Name reactions | |
| Corey–Kim oxidation Oxidation | The Corey–Kim oxidation is an oxidation reaction used to synthesize aldehydes and ketones from primary and secondary alcohols. It is named for American chemist and Nobel Laureate Elias James Corey and… | Wikipedia: Category:Name reactions | |
| Corey–Link reaction | In organic chemistry, the Corey–Link reaction is a name reaction that converts a 1,1,1-trichloro-2-keto structure into a 2-aminocarboxylic acid (an alpha amino acid) or other acyl functional group wit… | Wikipedia: Category:Name reactions | |
| Corey–Nicolaou macrolactonization | Corey–Nicolaou macrolactonization is a named reaction of organic chemistry, for the synthesis of lactones from hydroxy acids, found in 1974. The reaction uses 2,2'-dipyridyldisulfide and triphenylphos… | Wikipedia: Category:Name reactions |
