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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 |
|---|---|---|---|
| Kowalski ester homologation | The Kowalski ester homologation is a chemical reaction for the homologation of esters. | Wikipedia: Category:Name reactions | |
| Krapcho decarboxylation | Krapcho decarboxylation is a chemical reaction used to manipulate certain organic esters. This reaction applies to esters with a beta electron-withdrawing group (EWG). | Wikipedia: Category:Name reactions | |
| Kröhnke pyridine synthesis | Kröhnke pyridine synthesis is a reaction in organic synthesis that occurs between α-pyridinium methyl ketone salts and α, β-unsaturated carbonyl compounds and is used to generate highly functionalized… | Wikipedia: Category:Name reactions | |
| KRYPTOPYRROLE (Pyrrole, 2,4-dimethyl-3-ethyl) | Preparation of Pyrrole, 2,4-dimethyl-3-ethyl. Submitted by Hans Fischer. DOI: 10.15227/orgsyn.021.0067. | Organic Syntheses | |
| Kulinkovich reaction | The Kulinkovich reaction describes the organic synthesis of substituted cyclopropanols through reaction of esters with dialkyldialkoxytitanium reagents, which are generated in situ from Grignard rea… | Wikipedia: Category:Name reactions | |
| Kumada coupling Cross-coupling | In organic chemistry, the Kumada coupling is a type of cross coupling reaction, useful for generating carbon–carbon bonds by the reaction of a Grignard reagent and an organic halide. The procedure use… | Wikipedia: Category:Name reactions | |
| LACTAMIDE | Preparation of LACTAMIDE. Submitted by J. Kleinberg and L. F. Audrieth. DOI: 10.15227/orgsyn.021.0071. | Organic Syntheses | |
| l-ARABINOSE | Preparation of l-ARABINOSE. Submitted by Ernest Anderson and Lila Sands. DOI: 10.15227/orgsyn.008.0018. | Organic Syntheses | |
| LARGE SCALE, GREEN SYNTHESIS OF A GENERATION-1 MELAMINE (TRIAZINE) DENDRIMER | Preparation of LARGE SCALE, GREEN SYNTHESIS OF A GENERATION-1 MELAMINE (TRIAZINE) DENDRIMER. Submitted by Abdellatif Chouai, Vincent J. Venditto, and Eric E. Simanek1. DOI: 10.15227/orgsyn.086.0151. | Organic Syntheses | |
| Larock indole synthesis | The Larock indole synthesis is a heteroannulation reaction that uses palladium as a catalyst to synthesize indoles from an ortho-iodoaniline and a disubstituted alkyne. It is also known as Larock hete… | Wikipedia: Category:Name reactions | |
| LAURONE (12-Tricosanone) | Preparation of 12-Tricosanone. Submitted by J. C. Sauer1. DOI: 10.15227/orgsyn.031.0068. | Organic Syntheses | |
| LAURYL ALCOHOL (Dodecyl alcohol) | Preparation of Dodecyl alcohol. Submitted by S. G. Ford and C. S. Marvel. DOI: 10.15227/orgsyn.010.0062. | Organic Syntheses | |
| LAURYLMETHYLAMINE (Dodecylamine, N-methyl-) | Preparation of Dodecylamine, N-methyl-. Submitted by C. V. Wilson and J. F. Stenberg1. DOI: 10.15227/orgsyn.036.0048. | Organic Syntheses | |
| l-CYSTINE | Preparation of l-CYSTINE. Submitted by R. A. Gortner and W. F. Hoffman. DOI: 10.15227/orgsyn.005.0039. | Organic Syntheses | |
| Leblanc process | The Leblanc process was an early industrial process for making soda ash (sodium carbonate) used throughout the 19th century, named after its inventor, Nicolas Leblanc. It involved two stages: making … | Wikipedia: Category:Name reactions | |
| Lehmstedt–Tanasescu reaction | The Lehmstedt–Tanasescu reaction is a method in organic chemistry for the organic synthesis of acridone derivatives (3) from a 2-nitrobenzaldehyde (1) and an arene compound (2): | Wikipedia: Category:Name reactions | |
| Leimgruber–Batcho indole synthesis | The Leimgruber–Batcho indole synthesis is a series of organic reactions that produce indoles from o-nitrotoluenes 1.[1][2][3] The first step is the formation of an enamine 2 using N,N-dimethylformamid… | Wikipedia: Category:Name reactions | |
| Lemieux–Johnson oxidation Oxidation | The Lemieux–Johnson or Malaprade–Lemieux–Johnson oxidation is a chemical reaction in which an olefin undergoes oxidative cleavage to form two aldehyde or ketone units. The reaction is named after its … | Wikipedia: Category:Name reactions | |
| LEPIDINE | Preparation of LEPIDINE. Submitted by Fred W. Neumann, Nolan B. Sommer, C. E. Kaslow, and R. L. Shriner. DOI: 10.15227/orgsyn.026.0045. | Organic Syntheses | |
| Letts nitrile synthesis | The Letts nitrile synthesis is a chemical reaction of aromatic carboxylic acids with metal thiocyanates to form nitriles. The reaction includes the loss of carbon dioxide and potassium hydrosulfide. T… | Wikipedia: Category:Name reactions | |
| Leuckart reaction | The Leuckart reaction is the chemical reaction that converts aldehydes or ketones to amines. The reaction is an example of reductive amination. The reaction, named after Rudolf Leuckart, uses either a… | Wikipedia: Category:Name reactions | |
| Leuckart thiophenol reaction | The Leuckart thiophenol reaction is the decomposition of a diazoxanthate, by gentle warming in a slightly acidic cuprous medium, to its corresponding aryl xanthates which give aryl thiols on alkaline … | Wikipedia: Category:Name reactions | |
| LEVOPIMARIC ACID | Preparation of LEVOPIMARIC ACID. Submitted by Winston D. Lloyd and Glen W. Hedrick1. DOI: 10.15227/orgsyn.045.0064. | Organic Syntheses | |
| LEVULINIC ACID | Preparation of LEVULINIC ACID. Submitted by B. F. McKenzie. DOI: 10.15227/orgsyn.009.0050. | Organic Syntheses | |
| l-HISTIDINE MONOHYDROCHLORIDE | Preparation of l-HISTIDINE MONOHYDROCHLORIDE. Submitted by G. L. Foster and D. Shemin. DOI: 10.15227/orgsyn.018.0043. | Organic Syntheses | |
| Liebeskind–Srogl coupling Cross-coupling | The Liebeskind–Srogl coupling reaction is an organic reaction forming a new carbon–carbon bond from a thioester and a boronic acid using a metal catalyst. It is a cross-coupling reaction. This reactio… | Wikipedia: Category:Name reactions | |
| LIGAND-FREE COPPER(II) OXIDE NANOPARTICLES CATALYZED SYNTHESIS OF SUBSTITUTED BENZOXAZOLES | Preparation of LIGAND-FREE COPPER(II) OXIDE NANOPARTICLES CATALYZED SYNTHESIS OF SUBSTITUTED BENZOXAZOLES. Submitted by Prasenjit Saha, Md Ashif Ali, and Tharmalingam Punniyamurthy1. DOI: 10.15227/org… | Organic Syntheses | |
| Lindgren oxidation Oxidation | Lindgren oxidation is a selective method for oxidizing aldehydes to carboxylic acids. The reaction is named after Bengt O. Lindgren. | Wikipedia: Category:Name reactions | |
| LINOLEIC ACID | Preparation of LINOLEIC ACID. Submitted by J. W. McCutcheon. DOI: 10.15227/orgsyn.022.0075. | Organic Syntheses | |
| LINOLENIC ACID | Preparation of LINOLENIC ACID. Submitted by J. W. McCutcheon. DOI: 10.15227/orgsyn.022.0082. | Organic Syntheses | |
| LIPASE-CATALYZED KINETIC RESOLUTION OF ALCOHOLS VIA CHLOROACETATE ESTERS: (−)-(1R,2S)-trans-2-PHENYLCYCLOHEXANOL AND (+)-(1S,2R)-trans-2-PHENYLCYCLOHEXANOL (Cyclohexanol, 2-phenyl-, (1R-trans)- and cyclohexanol, 2-phenyl-, (1S-trans)-) | Preparation of Cyclohexanol, 2-phenyl-, (1R-trans)- and cyclohexanol, 2-phenyl-, (1S-trans)-. Submitted by A. Schwartz1, P. Madan1, J. K. Whitesell2, and R. M. Lawrence2. DOI: 10.15227/orgsyn.069.0001… | Organic Syntheses | |
| LIPASE-CATALYZED RESOLUTION OF 4-TRIMETHYLSILYL-3-BUTYN-2-OL AND CONVERSION OF THE (R)-ENANTIOMER TO (R)-3-BUTYN-2-YL MESYLATE AND (P)-1-TRIBUTYLSTANNYL-1,2-BUTADIENE (3-Butyn-2-ol, 4-(trimethylsilyl)-, (2R)- and Stannane, 1,2-butadienyltributyl-, (P)-) | Preparation of 3-Butyn-2-ol, 4-(trimethylsilyl)-, (2R)- and Stannane, 1,2-butadienyltributyl-, (P)-. Submitted by James A. Marshall and Harry Chobanian1. DOI: 10.15227/orgsyn.082.0043. | Organic Syntheses | |
| LITHIATED PRIMARY ALKYL CARBAMATES FOR THE HOMOLOGATION OF BORONIC ESTERS | Preparation of LITHIATED PRIMARY ALKYL CARBAMATES FOR THE HOMOLOGATION OF BORONIC ESTERS. Submitted by Matthew P. Webster, Benjamin M. Partridge, and Varinder K. Aggarwal.1. DOI: 10.15227/orgsyn.088.0… | Organic Syntheses | |
| LITHIUM AMIDES AS HOMOCHIRAL AMMONIA EQUIVALENTS FOR CONJUGATE ADDITIONS TO α,β-UNSATURATED ESTERS: ASYMMETRIC SYNTHESIS OF (S)-β-LEUCINE Addition | Preparation of LITHIUM AMIDES AS HOMOCHIRAL AMMONIA EQUIVALENTS FOR CONJUGATE ADDITIONS TO α,β-UNSATURATED ESTERS: ASYMMETRIC SYNTHESIS OF (S)-β-LEUCINE. Submitted by Stephen G. Davies1, Ai M. Fletche… | Organic Syntheses | |
| l-MENTHONE | Preparation of l-MENTHONE. Submitted by L. T. Sandborn. DOI: 10.15227/orgsyn.009.0052. | Organic Syntheses | |
| l-MENTHOXYACETIC ACID (Acetic acid, (menthyloxy)-, l-) | Preparation of Acetic acid, (menthyloxy)-, l-. Submitted by M. T. Leffler and A. E. Calkins. DOI: 10.15227/orgsyn.023.0052. | Organic Syntheses | |
| l-MENTHOXYACETYL CHLORIDE (Acetyl chloride, (menthyloxy)-, l-) | Preparation of Acetyl chloride, (menthyloxy)-, l-. Submitted by M. T. Leffler and A. E. Calkins. DOI: 10.15227/orgsyn.023.0055. | Organic Syntheses | |
| Lobry de Bruyn–Van Ekenstein transformation | In carbohydrate chemistry, the Lobry de Bruyn–Van Ekenstein transformation also known as the Lobry de Bruyn–Alberda van Ekenstein transformation is the base or acid catalyzed transformation of an aldo… | Wikipedia: Category:Name reactions | |
| Lombardo methylenation | In organic chemistry, the Lombardo methylenation is a name reaction that allows for the methylenation of carbonyl compounds with the use of Lombardo's reagent, which is a mix of zinc, dibromomethane, … | Wikipedia: Category:Name reactions | |
| Lossen rearrangement Rearrangement | The Lossen rearrangement is the conversion of an acyl hydroxamate to an isocyanate and carboxylic acid side product. The isocyanate can be used further to generate ureas in the presence of amines or g… | Wikipedia: Category:Name reactions | |
| Low-epimerization Peptide Bond Formation with Oxyma Pure: Preparation of Z-L-Phg-Val-OMe | Preparation of Low-epimerization Peptide Bond Formation with Oxyma Pure: Preparation of Z-L-Phg-Val-OMe. Submitted by Ramon Subirós-Funosas,* Ayman El-Faham*, and Fernando Albericio.* 1. DOI: 10.15227… | Organic Syntheses | |
| LOW PRESSURE CARBONYLATION OF EPOXIDES TO β-LACTONES | Preparation of LOW PRESSURE CARBONYLATION OF EPOXIDES TO β-LACTONES. Submitted by Submitted by John W. Kramer, Daniel S. Treitler, and Geoffrey W. Coates1. DOI: 10.15227/orgsyn.086.0287. | Organic Syntheses | |
| l-PROPYLENE GLYCOL (1,2-Propanediol, l-) | Preparation of 1,2-Propanediol, l-. Submitted by P. A. Levene and A. Walti. DOI: 10.15227/orgsyn.010.0084. | Organic Syntheses | |
| L-(S)-GLYCERALDEHYDE ACETONIDE (1,3-Dioxolane-4-carboxaldehyde, 2,2-dimethyl-, (S)-) | Preparation of 1,3-Dioxolane-4-carboxaldehyde, 2,2-dimethyl-, (S)-. Submitted by Christian Hubschwerlen, Jean-Luc Specklin, and J. Higelin1. DOI: 10.15227/orgsyn.072.0001. | Organic Syntheses | |
| l-TRYPTOPHANE (By-product, l-Tyrosine) | Preparation of By-product, l-Tyrosine. Submitted by Gerald J. Cox and Harriette King. DOI: 10.15227/orgsyn.010.0100. | Organic Syntheses | |
| Luche reduction Reduction | Luche reduction is the selective organic reduction of α,β-unsaturated ketones to allylic alcohols. The active reductant is described as "cerium borohydride", which is generated in situ from NaBH4 and … | Wikipedia: Category:Name reactions | |
| Lumière–Barbier method Organometallic addition | The Lumière–Barbier method is a method of acetylating aromatic amines in aqueous solutions. Illustrative is the acetylation of aniline. First aniline is dissolved in water using one equivalent of hyd… | Wikipedia: Category:Name reactions | |
| MACROCYCLIC DIIMINES: 1,10-DIAZACYCLOÖCTADECANE | Preparation of MACROCYCLIC DIIMINES: 1,10-DIAZACYCLOÖCTADECANE. Submitted by Chung Ho Park and Howard E. Simmons1. DOI: 10.15227/orgsyn.054.0088. | Organic Syntheses | |
| MACROCYCLIC POLYAMINES: 1,4,7,10,13,16-HEXAÄZACYCLOÖCTADECANE | Preparation of MACROCYCLIC POLYAMINES: 1,4,7,10,13,16-HEXAÄZACYCLOÖCTADECANE. Submitted by T. J. Atkins1, J. E. Richman, and W. F. Oettle. DOI: 10.15227/orgsyn.058.0086. | Organic Syntheses | |
| MACROCYCLIC POLYETHERS: DIBENZO-18-CROWN-6 POLYETHER AND DICYCLOHEXYL-18-CROWN-6 POLYETHER (Dibenzo [b,k] [1,4,7,10,13,16] hexaoxacycloöctadecin, 6,7,9,10,17,18,20,21-octahydro- and dibenzo [b,k] [1,4,7,10,13,16] hexaoxacycloöctadecin, eicosahydro-) | Preparation of Dibenzo [b,k] [1,4,7,10,13,16] hexaoxacycloöctadecin, 6,7,9,10,17,18,20,21-octahydro- and dibenzo [b,k] [1,4,7,10,13,16] hexaoxacycloöctadecin, eicosahydro-. Submitted by Charles J. Ped… | Organic Syntheses |
