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written by L. Kurti and B. Czako gives a detailed description,
background, mechanism, and applications of named reactions
commonly used in organic synthesis.
The book is a combination of 250 named reactions, arranged
alphabetically and compiled from a comprehensive and recent
literature.
A highly recommended book for research scholars working on
synthetic organic chemistry.
LIST OF NAMED REACTIONS
Acetoacetic Ester Synthesis
Acyloin Condensation
Alder (Ene) Reaction (Hydro-Allyl Addition)
Aldol Reaction
Alkene (Olefin) Metathesis
Alkyne Metathesis
Amadori Reaction/Rearrangement
Arbuzov Reaction (Michaelis-Arbuzov Reaction)
Arndt-Eistert Homologation/Synthesis
Aza-Claisen Rearrangement (3-Aza-Cope Rearrangement)
Aza-Cope Rearrangement
Aza-Wittig Reaction
Aza-[2,3]-Wittig Rearrangement
Baeyer-Villiger Oxidation/Rearrangement
Baker-Venkataraman Rearrangement
Baldwin’s Rules/Guidelines for Ring-Closing Reactions
Balz-Schiemann Reaction (Schiemann
Bamford-Stevens-Shapiro Olefination
Barbier Coupling Reaction
Bartoli Indole synthesis
Barton Nitrite Ester
Barton Radical Decarboxylation
Barton-McCombie Radical Deoxygenation Reaction
Baylis-Hillman Reaction
Beckmann Rearrangement
Benzilic Acid Rearrangement
Benzoin and Retro-Benzoin Condensation
Bergman Cycloaromatization Reaction
Biginelli Reaction
Birch Reduction
Bischler-Napieralski Isoquinoline Synthesis
Brook Rearrangement
Brown Hydroboration Reaction
Buchner Method of Ring Expansion (Buchner Reaction)
Buchwald-Hartwig Cross-Coupling
Burgess Dehydration Reaction
Cannizzaro Reaction
Carroll Rearrangement (Kimel-Cope Rearrangement)
Castro-Stephens Coupling
Chichibabin Amination Reaction (Chichibabin Reaction)
Chugaev Elimination Reaction (Xanthate Ester Pyrolysis)
Ciamician-Dennstedt Rearrangement
Claisen Condensation/Claisen Reaction
Claisen Rearrangement
Claisen-Ireland Rearrangement
Clemmensen Reduction
Combes Quinoline Synthesis
Cope Elimination / Cope Reaction
Cope Rearrangement
Corey-Bakshi-Shibata Reduction (CBS Reduction)
Corey-Chaykovsky Epoxidation and Cyclopropanation
Corey-Fuchs Alkyne Synthesis
Corey-Kim Oxidation
Corey-Nicolaou Macrolactonization
Corey-Winter Olefination
Cornforth Rearrangement
Criegee Oxidation
Curtius Rearrangement
Dakin Oxidation
Dakin-West Reaction
Danheiser Benzannulation
Danheiser Cyclopentene Annulation
Danishefsky’s Diene Cycloaddition
Darzens Glycidic Ester Condensation
Davis' Oxaziridine Oxidations
De Mayo Cycloaddition (Enone-Alkene [2+2] Photocycloaddition)
Demjanov Rearrangement and Tiffeneau-Demjanov Rearrangement
Dess-Martin Oxidation
Dieckmann Condensation
Diels-Alder Cycloaddition
Dienone-Phenol Rearrangement
Dimroth Rearrangement
Doering-LaFlamme Allene Synthesis
Dötz Benzannulation Reaction
Enders SAMP/RAMP Hydrazone Alkylation
Enyne Metathesis
Eschenmoser Methenylation
Eschenmoser-Claisen Rearrangement
Eschenmoser-Tanabe Fragmentation
Eschweiler-Clarke Methylation (Reductive Alkylation)
Evans Aldol Reaction
Favorskii and Homo-Favorskii Rearrangement
Feist-Bénary Furan Synthesis
Ferrier Reaction/Rearrangement
Finkelstein Reaction
Fischer Indole Synthesis
Fleming-Tamao Oxidation
Friedel-Crafts Acylation
Friedel-Crafts Alkylation
Fries-, Photo-Fries, and Anionic Ortho-Fries Rearrangement
Gabriel Synthesis
Gattermann and Gattermann-Koch Formylation
Glaser Coupling
Grignard Reaction
Grob Fragmentation
Hajos-Parrish Reaction
Hantzsch Dihydropyridine Synthesis
Heck Reaction
Heine Reaction
Hell-Volhard-Zelinsky Reaction
Henry Reaction
Hetero Diels-Alder Cycloaddition (HDA)
Hofmann Elimination
Hofmann-Löffler-Freytag Reaction (Remote Functionalization)
Hofmann Rearrangement
Horner-Wadsworth-Emmons Olefination
Horner-Wadsworth-Emmons Olefination – Still-Gennari Modification
Houben-Hoesch Reaction/Synthesis
Hunsdiecker Reaction
Jacobsen Hydrolytic Kinetic Resolution
Jacobsen-Katsuki Epoxidation
Japp-Klingemann Reaction
Johnson-Claisen Rearrangement
Jones Oxidation/Oxidation of Alcohols by Chromium Reagents
Julia-Lythgoe Olefination
Kagan-Molander Samarium Diiodide-Mediated Coupling
Kahne Glycosidation
Keck Asymmetric Allylation
Keck Macrolactonization
Keck Radical Allylation
Knoevenagel Condensation
Knorr Pyrrole Synthesis
Koenigs-Knorr Glycosidation
Kolbe-Schmitt Reaction
Kornblum Oxidation
Krapcho Dealkoxycarbonylation (Krapcho reaction)
Kröhnke Pyridine Synthesis
Kulinkovich Reaction
Kumada Cross-Coupling
Larock Indole Synthesis
Ley Oxidation
Lieben Haloform Reaction
Lossen Rearrangement
Luche Reduction
Madelung Indole Synthesis
Malonic Ester Synthesis
Mannich Reaction
McMurry Coupling
Meerwein Arylation
Meerwein-Ponndorf-Verley Reduction
Meisenheimer Rearrangement
Meyer-Schuster and Rupe Rearrangement
Michael Addition Reaction
Midland Alpine Borane Reduction
Minisci Reaction
Mislow-Evans Rearrangement
Mitsunobu Reaction
Miyaura Boration
Mukaiyama Aldol Reaction
Myers Asymmetric Alkylation
Nagata Hydrocyanation
Nazarov Cyclization
Neber Rearrangement
Nef Reaction
Negishi Cross-Coupling
Nenitzescu Indole Synthesis
Nicholas Reaction
Noyori Asymmetric Hydrogenation
Nozaki-Hiyama-Kishi Reaction
Oppenauer Oxidation
Overman Rearrangement
Oxy-Cope Rearrangement and Anionic Oxy-Cope Rearrangement
Paal-Knorr Furan Synthesis
Paal-Knorr Pyrrole Synthesis
Passerini Multicomponent Reaction
Paterno-Büchi Reaction
Pauson-Khand Reaction
Payne Rearrangement
Perkin Reaction
Petasis Boronic Acid-Mannich Reaction
Petasis-Ferrier Rearrangement
Peterson Olefination
Pfitzner-Moffatt Oxidation
Pictet-Spengler Tetrahydroisoquinoline Synthesis
Pinacol and Semipinacol Rearrangement
Pinner Reaction
Pinnick Oxidation
Polonovski Reaction
Pomeranz-Fritsch Reaction
Prévost Reaction
Prilezhaev Reaction
Prins Reaction
Prins-Pinacol Rearrangement
Pummerer Rearrangement
Quasi-Favorskii Rearrangement
Ramberg-Bäcklund Rearrangement
Reformatsky Reaction
Regitz Diazo Transfer
Reimer-Tiemann Reaction
Riley Selenium Dioxide Oxidation
Ritter Reaction
Robinson Annulation
Roush Asymmetric Allylation
Rubottom Oxidation
Saegusa Oxidation
Sakurai Allylation
Sandmeyer Reaction
Schmidt Reaction
Schotten-Baumann Reaction
Schwartz Hydrozirconation
Seyferth-Gilbert Homologation
Sharpless Asymmetric Aminohydroxylation
Sharpless Asymmetric Dihydroxylation
Sharpless Asymmetric Epoxidation
Shi Asymmetric Epoxidation
Simmons-Smith Cyclopropanation
Skraup and Doebner-Miller Quinoline Synthesis
Smiles Rearrangement
Smith-Tietze Multicomponent Dithiane Linchpin Coupling
Snieckus Directed Ortho Metalation
Sommelet-Hauser Rearrangement
Sonogashira Cross-Coupling
Staudinger Ketene Cycloaddition
Staudinger Reaction
Stephen Aldehyde Synthesis (Stephen Reduction)
Stetter Reaction
Stevens Rearrangement
Stille Carbonylative Cross-Coupling
Stille Cross-Coupling (Migita-Kosugi-Stille Coupling)
Stille-Kelly Coupling
Stobbe Condensation
Stork Enamine Synthesis
Strecker Reaction
Suzuki Cross-Coupling (Suzuki-Miyaura Cross-Coupling)
Swern Oxidation
Takai-Utimoto Olefination (Takai Reaction)
Tebbe Olefination/Petasis-Tebbe Olefination
Tishchenko Reaction
Tsuji-Trost Reaction/Allylation
Tsuji-Wilkinson Decarbonylation Reaction
Ugi Multicomponent Reaction
Ullmann Biaryl Ether and Biaryl Amine Synthesis/Condensation
Ullmann Reaction/Coupling/Biaryl Synthesis
Vilsmeier-Haack Formylation
Vinylcyclopropane-Cyclopentene Rearrangement
von Pechman Reaction
Wacker Oxidation
Wagner-Meerwein Rearrangement
Weinreb Ketone Synthesis.478
Wharton Fragmentation
Wharton Olefin Synthesis (Wharton Transposition)
Williamson Ether Synthesis
Wittig Reaction
Wittig Reaction - Schlosser Modification
Wittig-[1,2]- and [2,3]-Rearrangement
Wohl-Ziegler Bromination
Wolff Rearrangement
Wolff-Kishner Reduction
Wurtz Coupling
Yamaguchi Macrolactonization
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