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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 |
|---|---|---|---|
| CATALYST, RANEY NICKEL, W-2 | Preparation of CATALYST, RANEY NICKEL, W-2. Submitted by Ralph Mozingo. DOI: 10.15227/orgsyn.021.0015. | Organic Syntheses | |
| CATALYST, RANEY NICKEL, W-6 (With high contents of aluminum and adsorbed hydrogen) | Preparation of With high contents of aluminum and adsorbed hydrogen. Submitted by Harry R. Billica and Homer Adkins. DOI: 10.15227/orgsyn.029.0024. | Organic Syntheses | |
| CATALYTIC ASYMMETRIC ACYLATION OF ALCOHOLS USING A CHIRAL 1,2-DIAMINE DERIVED FROM (S)-PROLINE: (1S,2S)-trans-1-BENZOYLOXY-2-BROMOCYCLOHEXANE | Preparation of CATALYTIC ASYMMETRIC ACYLATION OF ALCOHOLS USING A CHIRAL 1,2-DIAMINE DERIVED FROM (S)-PROLINE: (1S,2S)-trans-1-BENZOYLOXY-2-BROMOCYCLOHEXANE. Submitted by Dai Terakado and Takeshi Oriy… | Organic Syntheses | |
| CATALYTIC ASYMMETRIC ACYL HALIDE-ALDEHYDE CYCLOCONDENSATION REACTION ((4S)-4-(2-Phenylethyl)-2-oxetanone) Condensation | Preparation of (4S)-4-(2-Phenylethyl)-2-oxetanone. Submitted by Scott G. Nelson and Paul M. Mills1. DOI: 10.15227/orgsyn.082.0170. | Organic Syntheses | |
| CATALYTIC ASYMMETRIC ADDITION OF AN IN-SITU PREPARED ARYLZINC TO CYCLOHEXANECARBOXALDEHYDE: (R)-(+)-α-CYCLOHEXYL-3-METHOXY-BENZENEMETHANOL Addition | Preparation of CATALYTIC ASYMMETRIC ADDITION OF AN IN-SITU PREPARED ARYLZINC TO CYCLOHEXANECARBOXALDEHYDE: (R)-(+)-α-CYCLOHEXYL-3-METHOXY-BENZENEMETHANOL. Submitted by Albert M. DeBerardinis, Mark Tur… | Organic Syntheses | |
| CATALYTIC ASYMMETRIC ALLYLATION REACTIONS: (S)-1-(PHENYLMETHOXY)-4-PENTEN-2-OL (4-Penten-2-ol, 1-(phenylmethoxy)-, (S)-) | Preparation of 4-Penten-2-ol, 1-(phenylmethoxy)-, (S)-. Submitted by Gary E. Keck1 and Dhileepkumar Krishnamurthy. DOI: 10.15227/orgsyn.075.0012. | Organic Syntheses | |
| CATALYTIC ASYMMETRIC SYNTHESIS OF NITROALDOLS USING A LANTHANUM-LITHIUM-BINOL COMPLEX: (2S,3S)-2-NITRO-5-PHENYL-1,3-PENTANEDIOL (L-threo-Pentitol, 1,2,4-trideoxy-4-nitro-1-phenyl-) Condensation | Preparation of L-threo-Pentitol, 1,2,4-trideoxy-4-nitro-1-phenyl-. Submitted by Hiroaki Sasai1a , Shizue Watanabe, Takeyuki Suzuki, and Masakatsu Shibasaki1b. DOI: 10.15227/orgsyn.078.0014. | Organic Syntheses | |
| CATALYTIC ENANTIOSELECTIVE ADDITION OF DIALKYLZINCS TO ALDEHYDES USING (2S)-(−)-3-exo-(DIMETHYLAMINO)ISOBORNEOL [(2S)-DAIB]: (S)-1-PHENYL-1-PROPANOL (Benzenemethanol, α-ethyl-, (S)-) Addition | Preparation of Benzenemethanol, α-ethyl-, (S)-. Submitted by Masato Kitamura, Hiromasa Oka, Seiji Suga, and Ryoji Noyori1. DOI: 10.15227/orgsyn.079.0139. | Organic Syntheses | |
| CATALYTIC ENANTIOSELECTIVE ADDITION OF TERMINAL ALKYNES TO ALDEHYDES: PREPARATION OF (S)-(-)-1,3-DIPHENYL-2-PROPYN-1-OL AND (S)-(-)-4-METHYL-1-PHENYL-2-PENTYN-1,4-DIOL Addition | Preparation of CATALYTIC ENANTIOSELECTIVE ADDITION OF TERMINAL ALKYNES TO ALDEHYDES: PREPARATION OF (S)-(-)-1,3-DIPHENYL-2-PROPYN-1-OL AND (S)-(-)-4-METHYL-1-PHENYL-2-PENTYN-1,4-DIOL. Submitted by Ryo… | Organic Syntheses | |
| CATALYTIC ENANTIOSELECTIVE BORANE REDUCTION OF BENZYL OXIMES: PREPARATION OF (S)-1-PYRIDIN-3-YL-ETHYLAMINE BIS HYDROCHLORIDE Reduction | Preparation of CATALYTIC ENANTIOSELECTIVE BORANE REDUCTION OF BENZYL OXIMES: PREPARATION OF (S)-1-PYRIDIN-3-YL-ETHYLAMINE BIS HYDROCHLORIDE. Submitted by Kun Huang and Margarita Ortiz-Marciales1. DOI:… | Organic Syntheses | |
| Catalytic Intramolecular Friedel-Crafts Reaction of Benzyl Meldrum's Acid Derivatives: Preparation of 5,6-Dimethoxy-2-Methyl-1-Indanone Electrophilic aromatic substitution | Preparation of Catalytic Intramolecular Friedel-Crafts Reaction of Benzyl Meldrum's Acid Derivatives: Preparation of 5,6-Dimethoxy-2-Methyl-1-Indanone. Submitted by Tiantong Lou, E-Ting Liao, Ashraf W… | Organic Syntheses | |
| CATALYTIC OSMIUM TETROXIDE OXIDATION OF OLEFINS: cis-1,2-CYCLOHEXANEDIOL Oxidation | Preparation of CATALYTIC OSMIUM TETROXIDE OXIDATION OF OLEFINS: cis-1,2-CYCLOHEXANEDIOL. Submitted by V. VanRheenen, D. Y. Cha, and W. M. Hartley1. DOI: 10.15227/orgsyn.058.0043. | Organic Syntheses | |
| CATALYTIC REDUCTION OF AMIDES TO AMINES WITH HYDROSILANES USING A TRIRUTHENIUM CARBONYL CLUSTER AS THE CATALYST Reduction | Preparation of CATALYTIC REDUCTION OF AMIDES TO AMINES WITH HYDROSILANES USING A TRIRUTHENIUM CARBONYL CLUSTER AS THE CATALYST. Submitted by Yukihiro Motoyama, Chikara Itonaga, Toshiki Ishida, Mikihir… | Organic Syntheses | |
| CATECHOL (Pyrocatechol) | Preparation of Pyrocatechol. Submitted by H. D. Dakin. DOI: 10.15227/orgsyn.003.0028. | Organic Syntheses | |
| Catellani reaction | The Catellani reaction was discovered by Marta Catellani (Università degli Studi di Parma, Italy) and co-workers in 1997. The reaction uses aryl iodides to perform bi- or tri-functionalization, includ… | Wikipedia: Category:Name reactions | |
| CELLOBIOSE | Preparation of CELLOBIOSE. Submitted by Géza Braun. DOI: 10.15227/orgsyn.017.0034. | Organic Syntheses | |
| CETYLMALONIC ESTER (Malonic acid, cetyl-, diethyl ester) | Preparation of Malonic acid, cetyl-, diethyl ester. Submitted by Don E. Floyd and Sidney E. Miller1. DOI: 10.15227/orgsyn.034.0013. | Organic Syntheses | |
| CHAIN ELONGATION OF ALKENES via gem-DIHALOCYCLOPROPANES: 2-BROMO-3,3-DIPHENYL-2-PROPEN-1-YL ACETATE (2-Propen-1-ol, 2-bromo-3,3-diphenyl-, acetate) | Preparation of 2-Propen-1-ol, 2-bromo-3,3-diphenyl-, acetate. Submitted by Stanely R. Sandler1. DOI: 10.15227/orgsyn.056.0032. | Organic Syntheses | |
| Chan–Lam coupling Cross-coupling | The Chan–Lam coupling reaction, also known as the Chan–Evans–Lam coupling, is a cross-coupling reaction between an aryl boronic acid and an alcohol or an amine to form the corresponding secondary aryl… | Wikipedia: Category:Name reactions | |
| Chan rearrangement Rearrangement | The Chan rearrangement is a chemical reaction that involves rearranging an acyloxy acetate (1) in the presence of a strong base to a 2-hydroxy-3-keto-ester (2).[1] | Wikipedia: Category:Name reactions | |
| Chapman rearrangement Rearrangement | The Chapman rearrangement is the thermal conversion of aryl N-arylbenzimidates to the corresponding amides, via intramolecular migration of an aryl group from oxygen to nitrogen. It is named after Art… | Wikipedia: Category:Name reactions | |
| CHELIDONIC ACID | Preparation of CHELIDONIC ACID. Submitted by E. Raymond Riegel and F. Zwilgmeyer. DOI: 10.15227/orgsyn.017.0040. | Organic Syntheses | |
| Chichibabin pyridine synthesis | The Chichibabin pyridine synthesis () is a method for synthesizing pyridine rings. The reaction involves the condensation reaction of aldehydes, ketones, α,β-unsaturated carbonyl compounds, or any com… | Wikipedia: Category:Name reactions | |
| CHIRAL 1,3-OXATHIANE FROM (+)-PULEGONE: HEXAHYDRO-4,4,7-TRIMETHYL-4H-1,3-BENZOXATHIIN (4H-1,3-Benzoxathiin, hexahydro-4,4,7-trimethyl-) | Preparation of 4H-1,3-Benzoxathiin, hexahydro-4,4,7-trimethyl-. Submitted by Ernest L. Eliel, Joseph E. Lynch, Fumitaka Kume, and Stephen V. Frye1. DOI: 10.15227/orgsyn.065.0215. | Organic Syntheses | |
| CHIRAL (ACYLOXY)BORANE COMPLEX-CATALYZED ASYMMETRIC DIELS-ALDER REACTION: (1R)-1,3,4-TRIMETHYL-3-CYCLOHEXENE-1-CARBOXALDEHYDE (3-Cyclohexene-1-carboxaldehyde, 1,3,4-trimethyl-, (−)-) | Preparation of 3-Cyclohexene-1-carboxaldehyde, 1,3,4-trimethyl-, (−)-. Submitted by Kyoji Furuta, Qing-Zhi Gao, and Hisashi Yamamoto1. DOI: 10.15227/orgsyn.072.0086. | Organic Syntheses | |
| CHIRAL LITHIUM AMIDE BASE DESYMMETRIZATION OF A RING FUSED IMIDE: FORMATION OF (3aS,7aS)-2-[2-(3,4-DIMETHOXYPHENYL)-ETHYL]-1,3-DIOXO-OCTAHYDRO-ISOINDOLE-3a-CARBOXYLIC ACID METHYL ESTER | Preparation of CHIRAL LITHIUM AMIDE BASE DESYMMETRIZATION OF A RING FUSED IMIDE: FORMATION OF (3aS,7aS)-2-[2-(3,4-DIMETHOXYPHENYL)-ETHYL]-1,3-DIOXO-OCTAHYDRO-ISOINDOLE-3a-CARBOXYLIC ACID METHYL ESTER.… | Organic Syntheses | |
| CHIRAL MEDIA FOR ASYMMETRIC SOLVENT INDUCTIONS. (S,S)-( + )-1,4-BIS(DIMETHYLAMINO)-2,3-DIMETHOXYBUTANE FROM (R,R)-( + )-DIETHYL TARTRATE (1,4-Butanediamine, 2,3-dimethoxy-N,N,N',N'-tetramethyl-[S,S]-) | Preparation of 1,4-Butanediamine, 2,3-dimethoxy-N,N,N',N'-tetramethyl-[S,S]-. Submitted by Dieter Seebach, Hans-Otto Kalinowski, Werner Langer, Gerhard Crass, and Eva-Maria Wilka1. DOI: 10.15227/orgsy… | Organic Syntheses | |
| CHLOROACETAMIDE (Acetamide, α-chloro-) | Preparation of Acetamide, α-chloro-. Submitted by W. A. Jacobs and M. Heidelberger. DOI: 10.15227/orgsyn.007.0016. | Organic Syntheses | |
| CHLOROACETONITRILE (Acetonitrile, chloro-) | Preparation of Acetonitrile, chloro-. Submitted by D. B. Reisner and E. C. Horning1. DOI: 10.15227/orgsyn.030.0022. | Organic Syntheses | |
| CHLORODIISOPROPYLPHOSPHINE (Phosphinous chloride, diisopropyl-) | Preparation of Phosphinous chloride, diisopropyl-. Submitted by W. Voskuil and J. F. Arens1. DOI: 10.15227/orgsyn.048.0047. | Organic Syntheses | |
| CHLOROMETHYLPHOSPHONOTHIOIC DICHLORIDE | Preparation of CHLOROMETHYLPHOSPHONOTHIOIC DICHLORIDE. Submitted by R. Schmutzler1. DOI: 10.15227/orgsyn.046.0021. | Organic Syntheses | |
| CHLORO-p-BENZOQUINONE (p-Benzoquinone, chloro-) | Preparation of p-Benzoquinone, chloro-. Submitted by R. E. Harman1. DOI: 10.15227/orgsyn.035.0022. | Organic Syntheses | |
| CHLOROSULFONYL ISOCYANATE (Isocyanic acid, anhydride with chlorosulfonic acid) | Preparation of Isocyanic acid, anhydride with chlorosulfonic acid. Submitted by Roderich Graf1. DOI: 10.15227/orgsyn.046.0023. | Organic Syntheses | |
| CHOLANE-24-AL | Preparation of CHOLANE-24-AL. Submitted by John G. Moffatt1. DOI: 10.15227/orgsyn.047.0025. | Organic Syntheses | |
| CHOLESTANONE | Preparation of CHOLESTANONE. Submitted by William F. Bruce. DOI: 10.15227/orgsyn.017.0043. | Organic Syntheses | |
| CHOLESTANYL METHYL ETHER (Cholestane, 3β-methoxy-) | Preparation of Cholestane, 3β-methoxy-. Submitted by M. Neeman1,2 and William S. Johnson1. DOI: 10.15227/orgsyn.041.0009. | Organic Syntheses | |
| CHOLESTENONE | Preparation of CHOLESTENONE. Submitted by R. V. Oppenauer. DOI: 10.15227/orgsyn.021.0018. | Organic Syntheses | |
| CHOLESTEROL, Δ5-CHOLESTEN-3-ONE, AND Δ4-CHOLESTEN-3-ONE (Cholesterol, Cholest-5-en-3-one, and Cholest-4-en-3-one) | Preparation of Cholesterol, Cholest-5-en-3-one, and Cholest-4-en-3-one. Submitted by Louis F. Fieser1. DOI: 10.15227/orgsyn.035.0043. | Organic Syntheses | |
| Chugaev elimination Elimination | The Chugaev elimination is a chemical reaction that involves the net removal of water from alcohols to produce alkenes. The intermediate is a xanthate. It is named for its discoverer, the Russian chem… | Wikipedia: Category:Name reactions | |
| Ciamician–Dennstedt rearrangement Rearrangement | The Ciamician–Dennstedt rearrangement is a name reaction in organic chemistry. It was first published in 1881 by the Italian chemist Giacomo Luigi Ciamician and his German colleague Max Dennstedt. The… | Wikipedia: Category:Name reactions | |
| CINNAMONITRILE (2-Propenenitrile, 3-phenyl-) | Preparation of 2-Propenenitrile, 3-phenyl-. Submitted by G. Lohaus1. DOI: 10.15227/orgsyn.050.0018. | Organic Syntheses | |
| CINNAMYL BROMIDE (Benzene, 3-bromopropenyl-) | Preparation of Benzene, 3-bromopropenyl-. Submitted by John P. Schaefer, J. G. Higgins, and P. K. Shenoy1. DOI: 10.15227/orgsyn.048.0051. | Organic Syntheses | |
| cis-2-BENZYL-3-PHENYLAZIRIDINE (Aziridine, 2-benzyl-3-phenyl-, cis-) | Preparation of Aziridine, 2-benzyl-3-phenyl-, cis-. Submitted by Katsumi Kotera and Keizo Kitahonoki1. DOI: 10.15227/orgsyn.048.0020. | Organic Syntheses | |
| cis-2-PHENYLCYCLOPROPANECARBOXYLIC ACID (Cyclopropanecarboxylic acid, 2-phenyl-, cis-) | Preparation of Cyclopropanecarboxylic acid, 2-phenyl-, cis-. Submitted by Carl Kaiser, Joseph Weinstock1, and M. P. Olmstead. DOI: 10.15227/orgsyn.050.0094. | Organic Syntheses | |
| cis-3,4-DICHLOROCYCLOBUTENE (Cyclobutene, 3,4-dichloro, cis-) | Preparation of Cyclobutene, 3,4-dichloro, cis-. Submitted by R. Pettit1 and J. Henery. DOI: 10.15227/orgsyn.050.0036. | Organic Syntheses | |
| cis-4-tert-BUTYLCYCLOHEXANOL (Cyclohexanol, 4-(1,1-dimethylethyl)-, cis-) | Preparation of Cyclohexanol, 4-(1,1-dimethylethyl)-, cis-. Submitted by E. L. Eliel1, T. W. Doyle, R. O. Hutchins2, and E. C. Gilbert. DOI: 10.15227/orgsyn.050.0013. | Organic Syntheses | |
| cis- AND trans-1,2-DIVINYLCYCLOBUTANE | Preparation of cis- AND trans-1,2-DIVINYLCYCLOBUTANE. Submitted by Charles D. DeBoer1, Nicholas J. Turro2, and George S. Hammond1. DOI: 10.15227/orgsyn.047.0064. | Organic Syntheses | |
| cis-CYCLODODECENE | Preparation of cis-CYCLODODECENE. Submitted by Masaji Ohno and Masaru Okamoto1. DOI: 10.15227/orgsyn.049.0030. | Organic Syntheses | |
| cis-DICHLOROALKANES FROM EPOXIDES: cis-1,2-DICHLOROCYCLOHEXANE (Cyclohexane, 1,2-dichloro-, cis-) | Preparation of Cyclohexane, 1,2-dichloro-, cis-. Submitted by James E. Oliver1 and Philip E. Sonnet2. DOI: 10.15227/orgsyn.058.0064. | Organic Syntheses | |
| cis-N-TOSYL-3-METHYL-2-AZABICYCLO[3.3.0]OCT-3-ENE (Cyclopenta[b]pyrrole, 1,3a,4,5,6,6a-hexahydro-2-methyl-1-[4-methylphenyl)sulfonyl]-, cis-) | Preparation of Cyclopenta[b]pyrrole, 1,3a,4,5,6,6a-hexahydro-2-methyl-1-[4-methylphenyl)sulfonyl]-, cis-. Submitted by Louis S. Hegedus, Michael S. Holden, and James M. McKearin1. DOI: 10.15227/orgsyn… | Organic Syntheses |
