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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 |
|---|---|---|---|
| CYCLOPENTANONE ANNULATION VIA CYCLOPROPANONE DERIVATIVES: (3aβ,9bβ)-1,2,3a,4,5,9b-HEXAHYDRO-9b-HYDROXY-3a-METHYL-3H-BENZ[e]INDEN-3-ONE Cyclization | Preparation of CYCLOPENTANONE ANNULATION VIA CYCLOPROPANONE DERIVATIVES: (3aβ,9bβ)-1,2,3a,4,5,9b-HEXAHYDRO-9b-HYDROXY-3a-METHYL-3H-BENZ[e]INDEN-3-ONE. Submitted by Michael J. Bradlee and Paul Helquist… | Organic Syntheses | |
| CYCLOPENTANONES FROM CARBOXYLIC ACIDS VIA INTRAMOLECULAR ACYLATION OF ALKYLSILANES: 2-METHYL-2-VINYLCYCLOPENTANONE (Cyclopentanone, 2-ethenyl-2-methyl-) | Preparation of Cyclopentanone, 2-ethenyl-2-methyl-. Submitted by Isao Kuwajima and Hirokazu Urabe1. DOI: 10.15227/orgsyn.066.0087. | Organic Syntheses | |
| CYCLOPENTENONES FROM α,α'-DIBROMOKETONES AND ENAMINES: 2,5-DIMETHYL-3-PHENYL-2-CYCLOPENTEN-1-ONE (2-Cyclopenten-1-one, 2,5-dimethyl-3-phenyl-) | Preparation of 2-Cyclopenten-1-one, 2,5-dimethyl-3-phenyl-. Submitted by R. Noyori1, K. Yokoyama, and Y. Hayakawa. DOI: 10.15227/orgsyn.058.0056. | Organic Syntheses | |
| CYCLOPROPANATION USING AN IRON-CONTAINING METHYLENE TRANSFER REAGENT: 1,1-DIPHENYLCYCLOPROPANE (Iron (1+), dicarbonyl(η5-2,4-cyclopentadien-1-yl)(dimethylsulfonium η-methylide)-, tetrafluoroborate (1-) and Benzene, 1,1'-cyclopropylidenebis-) | Preparation of Iron (1+), dicarbonyl(η5-2,4-cyclopentadien-1-yl)(dimethylsulfonium η-methylide)-, tetrafluoroborate (1-) and Benzene, 1,1'-cyclopropylidenebis-. Submitted by Matthew N. Mattson1, Edwar… | Organic Syntheses | |
| CYCLOPROPANECARBOXALDEHYDE | Preparation of CYCLOPROPANECARBOXALDEHYDE. Submitted by J. P. Barnier, J. Champion, and J. M. Conia1. DOI: 10.15227/orgsyn.060.0025. | Organic Syntheses | |
| CYCLOPROPANECARBOXYLIC ACID | Preparation of CYCLOPROPANECARBOXYLIC ACID. Submitted by Chester M. McCloskey and George H. Coleman. DOI: 10.15227/orgsyn.024.0036. | Organic Syntheses | |
| CYCLOPROPANONE ETHYL HEMIACETAL FROM ETHYL 3-CHLOROPROPANOATE (Cyclopropanol, 1-ethoxy-) | Preparation of Cyclopropanol, 1-ethoxy-. Submitted by J. Salaün and J. Marguerite1. DOI: 10.15227/orgsyn.063.0147. | Organic Syntheses | |
| CYCLOPROPENE: A NEW SIMPLE SYNTHESIS AND ITS DIELS-ALDER REACTION WITH CYCLOPENTADIENE (Tricyclo[3.2.1.02,4]oct-6-ene, (1α,2α,4α,5α)-) | Preparation of Tricyclo[3.2.1.02,4]oct-6-ene, (1α,2α,4α,5α)-. Submitted by Paul Binger1 , Petra Wedemann1 , and Udo H. Brinker2. DOI: 10.15227/orgsyn.077.0254. | Organic Syntheses | |
| CYCLOPROPENONE | Preparation of CYCLOPROPENONE. Submitted by R. Breslow1, J. Pecoraro, and T. Sugimoto. DOI: 10.15227/orgsyn.057.0041. | Organic Syntheses | |
| CYCLOPROPYLACETYLENE (Cyclopropane, ethynyl-) | Preparation of Cyclopropane, ethynyl-. Submitted by Edward G. Corley, Andrew S. Thompson, and Martha Huntington1. DOI: 10.15227/orgsyn.077.0231. | Organic Syntheses | |
| CYCLOPROPYLBENZENE (Benzene, cyclopropyl-) | Preparation of Benzene, cyclopropyl-. Submitted by Thomas F. Corbin, Roger C. Hahn1, and Harold Shechter2. DOI: 10.15227/orgsyn.044.0030. | Organic Syntheses | |
| CYCLOPROPYL CYANIDE (Cyclopropane, cyano-) | Preparation of Cyclopropane, cyano-. Submitted by M. J. Schlatter. DOI: 10.15227/orgsyn.023.0020. | Organic Syntheses | |
| CYCLOPROPYLDIPHENYLSULFONIUM TETRAFLUOROBORATE (Sulfonium, cyclopropyldiphenyl tetrafluoroborate(1-)) | Preparation of Sulfonium, cyclopropyldiphenyl tetrafluoroborate(1-). Submitted by Mitchell J. Bogdanowicz and Barry M. Trost1. DOI: 10.15227/orgsyn.054.0027. | Organic Syntheses | |
| CYCLOUNDECANECARBOXYLIC ACID | Preparation of CYCLOUNDECANECARBOXYLIC ACID. Submitted by Yasumasa Hamada and Takayuki Shioiri1. DOI: 10.15227/orgsyn.062.0191. | Organic Syntheses | |
| CYSTEIC ACID MONOHYDRATE | Preparation of CYSTEIC ACID MONOHYDRATE. Submitted by H. T. Clarke. DOI: 10.15227/orgsyn.020.0023. | Organic Syntheses | |
| (−)-D-2,10-CAMPHORSULTAM (3H-3a,6-Methano-2,1-benzisothiazole, 4,5,6,7-tetrahydro-8,8-dimethyl-2,2-dioxide, (3aS)-) | Preparation of 3H-3a,6-Methano-2,1-benzisothiazole, 4,5,6,7-tetrahydro-8,8-dimethyl-2,2-dioxide, (3aS)-. Submitted by Michael C. Weismiller, James C. Towson, and Franklin A. Davis1. DOI: 10.15227/orgs… | Organic Syntheses | |
| D-2-OXO-7,7-DIMETHYL-1-VINYLBICYCLO[2.2.1]HEPTANE (2-Norbornanone, 7,7-dimethyl-1-vinyl-, D-) | Preparation of 2-Norbornanone, 7,7-dimethyl-1-vinyl-, D-. Submitted by Nikolaus Fischer1 and G. Opitz2. DOI: 10.15227/orgsyn.048.0106. | Organic Syntheses | |
| DABCO-bis(sulfur dioxide), DABSO, as an easy-to-handle source of SO2: Sulfonamide preparation | Preparation of DABCO-bis(sulfur dioxide), DABSO, as an easy-to-handle source of SO2: Sulfonamide preparation. Submitted by Edward J. Emmett and Michael C. Willis1*. DOI: 10.15227/orgsyn.091.0125. | Organic Syntheses | |
| Dakin oxidation Oxidation | The Dakin oxidation (or Dakin reaction) is an organic redox reaction in which an ortho- or para-hydroxylated phenyl aldehyde (2-hydroxybenzaldehyde or 4-hydroxybenzaldehyde) or ketone reacts with hyd… | Wikipedia: Category:Name reactions | |
| Dakin–West reaction | The Dakin–West reaction is a chemical reaction that transforms an amino-acid into a keto-amide using an acid anhydride and a base, typically pyridine. It is named for Henry Drysdale Dakin and Randolph… | Wikipedia: Category:Name reactions | |
| d- and l-OCTANOL-2 (2-Octanol, d- and l-) | Preparation of 2-Octanol, d- and l-. Submitted by Joseph Kenyon. DOI: 10.15227/orgsyn.006.0068. | Organic Syntheses | |
| d- AND l-α-PHENYLETHYLAMINE (Benzylamine, α-methyl-, d- and l-) | Preparation of Benzylamine, α-methyl-, d- and l-. Submitted by A. W. Ingersoll. DOI: 10.15227/orgsyn.017.0080. | Organic Syntheses | |
| Danheiser annulation Cyclization | The Danheiser annulation or Danheiser TMS-cyclopentene annulation is an organic reaction of an α,β-unsaturated ketone and a trialkylsilylallene (e.g., trimethylsilyl- or triisopropylsilyl-) in the pre… | Wikipedia: Category:Name reactions | |
| Danheiser benzannulation Cyclization | The Danheiser benzannulation is a chemical reaction used in organic chemistry to generate highly substituted phenols in a single step. It is named after Rick L. Danheiser who developed the reaction. | Wikipedia: Category:Name reactions | |
| D-ARABINOSE | Preparation of D-ARABINOSE. Submitted by Géza Braun. DOI: 10.15227/orgsyn.020.0014. | Organic Syntheses | |
| d-ARGININE HYDROCHLORIDE | Preparation of d-ARGININE HYDROCHLORIDE. Submitted by E. Brand and M. Sandberg. DOI: 10.15227/orgsyn.012.0004. | Organic Syntheses | |
| Darzens halogenation Halogenation | Darzens halogenation is the chemical synthesis of alkyl halides from alcohols via the treatment upon reflux of a large excess of thionyl chloride or thionyl bromide (SOX2) in the presence of a small a… | Wikipedia: Category:Name reactions | |
| Darzens reaction | The Darzens reaction (also known as the Darzens condensation or glycidic ester condensation) is the chemical reaction of a ketone or aldehyde with an α-haloester in the presence of a base to form an α… | Wikipedia: Category:Name reactions | |
| Davis–Beirut reaction | The Davis–Beirut reaction is N,N-bond forming heterocyclization that creates numerous types of 2H-indazoles and indazolones in both acidic and basic conditions | Wikipedia: Category:Name reactions | |
| Davis oxidation Oxidation | In organic chemistry, the Davis oxidation or Davis' oxaziridine oxidation refers to oxidations involving the use of the Davis reagent (2-(phenylsulfonyl)-3-phenyloxaziridine) or other similar oxazirid… | Wikipedia: Category:Name reactions | |
| DEAMINATION OF AMINES. 2-PHENYLETHYL BENZOATE VIA THE NITROSOAMIDE DECOMPOSITION (Benzoic acid, 2-phenylethyl ester) | Preparation of Benzoic acid, 2-phenylethyl ester. Submitted by Emil White1. DOI: 10.15227/orgsyn.047.0044. | Organic Syntheses | |
| Debus–Radziszewski imidazole synthesis | The Debus–Radziszewski imidazole synthesis is a multi-component reaction used for the synthesis of imidazoles from a 1,2-dicarbonyl, an aldehyde, and ammonia or a primary amine. The method is used com… | Wikipedia: Category:Name reactions | |
| DECAMETHYLENE BROMIDE (Decane, 1,10-dibromo-) | Preparation of Decane, 1,10-dibromo-. Submitted by W. L. McEwen. DOI: 10.15227/orgsyn.020.0024. | Organic Syntheses | |
| DECAMETHYLENEDIAMINE (1,10-Decanediamine) | Preparation of 1,10-Decanediamine. Submitted by B. S. Biggs and W. S. Bishop. DOI: 10.15227/orgsyn.027.0018. | Organic Syntheses | |
| DECAMETHYLENE GLYCOL (1,10-Decanediol) | Preparation of 1,10-Decanediol. Submitted by R. H. Manske. DOI: 10.15227/orgsyn.014.0020. | Organic Syntheses | |
| DEHYDROACETIC ACID | Preparation of DEHYDROACETIC ACID. Submitted by F. Arndt. DOI: 10.15227/orgsyn.020.0026. | Organic Syntheses | |
| DEHYDROXYLATION OF PHENOLS; HYDROGENOLYSIS OF PHENOLIC ETHERS: BIPHENYL | Preparation of DEHYDROXYLATION OF PHENOLS; HYDROGENOLYSIS OF PHENOLIC ETHERS: BIPHENYL. Submitted by Walter J. Musliner and John W. Gates Jr1. DOI: 10.15227/orgsyn.051.0082. | Organic Syntheses | |
| De Kimpe aziridine synthesis | The De Kimpe aziridine synthesis is a name reaction of organic chemistry, for the generation of aziridines by the reaction of α-chloroimines with nucleophiles such as hydride, cyanide, or Grignard rea… | Wikipedia: Category:Name reactions | |
| Delépine reaction | The Delépine reaction is the organic synthesis of primary amines (4) by reaction of benzyl or alkyl halides (1) with hexamethylenetetramine (2) followed by acid hydrolysis of the quaternary ammonium s… | Wikipedia: Category:Name reactions | |
| DeMayo reaction | The DeMayo reaction or Ciamician-DeMayo reaction is a photochemical reaction in which the enol of a 1,3-diketone reacts with an alkene (or another species with a C=C bond) and the resulting cyclobutan… | Wikipedia: Category:Name reactions | |
| DEMETHYLATION OF METHYL ARYL ETHERS: 4-ETHOXY-3-HYDROXYBENZALDEHYDE (Benzaldehyde, 4-ethoxy-3-hydroxy-) | Preparation of Benzaldehyde, 4-ethoxy-3-hydroxy-. Submitted by Robert E. Ireland1 and David M. Walba2. DOI: 10.15227/orgsyn.056.0044. | Organic Syntheses | |
| Demjanov rearrangement Rearrangement | The Demjanov rearrangement is the chemical reaction of primary amines with nitrous acid to give rearranged alcohols.[1][2][3] It involves substitution by a hydroxyl group with a possible ring expansio… | Wikipedia: Category:Name reactions | |
| DEOXYANISOIN (Acetophenone, 4'-methoxy-2-(p-methoxyphenyl)-) | Preparation of Acetophenone, 4'-methoxy-2-(p-methoxyphenyl)-. Submitted by P. H. Carter, J. Cymerman Craig, Ruth E. Lack, and M. Moyle1. DOI: 10.15227/orgsyn.040.0016. | Organic Syntheses | |
| DEOXYGENATION OF EPOXIDES WITH LOWER VALENT TUNGSTEN HALIDES: trans-CYCLODODECENE | Preparation of DEOXYGENATION OF EPOXIDES WITH LOWER VALENT TUNGSTEN HALIDES: trans-CYCLODODECENE. Submitted by Martha A. Umbreit and K. Barry Sharpless1. DOI: 10.15227/orgsyn.060.0029. | Organic Syntheses | |
| DEOXYGENATION OF SECONDARY ALCOHOLS: 3-DEOXY-1,2:5,6-DI-O-ISOPROPYLIDENE-α-d-ribo-HEXOFURANOSE (α-d-ribo-Hexofuranose, 3-deoxy-1,2:5,6-bis-O-(1-methylethylidene)-) | Preparation of α-d-ribo-Hexofuranose, 3-deoxy-1,2:5,6-bis-O-(1-methylethylidene)-. Submitted by S. Iacono and James R. Rasmussen1. DOI: 10.15227/orgsyn.064.0057. | Organic Syntheses | |
| DESOXYBENZOIN | Preparation of DESOXYBENZOIN. Submitted by C. F. H. Allen and W. E. Barker. DOI: 10.15227/orgsyn.012.0016. | Organic Syntheses | |
| Dess–Martin oxidation Oxidation | The Dess–Martin oxidation is an organic reaction for the oxidation of primary alcohols to aldehydes and secondary alcohols to ketones using Dess–Martin periodinane. | Wikipedia: Category:Name reactions | |
| DESYL CHLORIDE (Acetophenone, α-chloro-α-phenyl-) | Preparation of Acetophenone, α-chloro-α-phenyl-. Submitted by A. M. Ward. DOI: 10.15227/orgsyn.012.0020. | Organic Syntheses | |
| DETRIFLUOROACETYLATIVE DIAZO GROUP TRANSFER: (E)-1-DIAZO-4-PHENYL-3-BUTEN-2-ONE (3-Buten-2-one, 1-diazo-4-phenyl-) | Preparation of 3-Buten-2-one, 1-diazo-4-phenyl-. Submitted by Rick L. Danheiser, Raymond F. Miller, and Ronald G. Brisbois1. DOI: 10.15227/orgsyn.073.0134. | Organic Syntheses | |
| Devarda's alloy | Devarda's alloy (CAS # 8049-11-4) is an alloy of aluminium (44% – 46%), copper (49% – 51%) and zinc (4% – 6%). | Wikipedia: Category:Name reactions |
