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Name reactions : a collection of detailed mechanisms and synthetic applications

Author: Jie Jack Li
Publisher: Berlin : Springer-Verlag, ©2009.
Edition/Format:   eBook : Document : English : 4th expanded edView all editions and formats
Database:WorldCat
Summary:

The revolutionary format of this fourth edition book covers over 300 classical as well as contemporary name reactions. Unlike other books on name reactions in organic chemistry, this book focuses on  Read more...

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Additional Physical Format: Print version:
Li, Jie Jack.
Name reactions.
Berlin : Springer-Verlag, ©2009
(DLC) 2009931220
(OCoLC)382399970
Material Type: Document, Internet resource
Document Type: Internet Resource, Computer File
All Authors / Contributors: Jie Jack Li
ISBN: 9783642010538 3642010539
OCLC Number: 615830762
Description: 1 online resource (xxii, 621 pages) : illustrations
Contents: Alder ene reaction.- Aldol condensation.- Algar- Flynn- Oyamada Reaction.- Allan-Robinson reaction.- Arndt-Eistert homologation.- Baeyer-Villiger oxidation.- Baker-Venkataraman rearrangement.- Bamford-Stevens reaction.- Barbier coupling reaction.- Bartoli indole synthesis.- Barton radical decarboxylation.- Barton-McCombie deoxygenation.- Barton nitrite photolysis.- Batcho-Leimgruber indole synthesis.- Baylis-Hillman reaction.- Beckmann rearrangement.- Benzilic acid rearrangement.- Benzoin condensation.- Bergman cyclization.- Biginelli pyrimidone synthesis.- Birch reduction.- Bischler-Mohlau indole synthesis.- Bischler-Napieralski reaction.- Blaise reaction.- Blum-Ittah aziridine synthesis.- Boekelheide reaction.- Boger pyridine synthesis.- Borch reductive amination.- Borsche-Drechsel cyclizations.- Boulton-Katritzky rearrangement.- Bouveault aldehyde synthesis.- Bouveault-Blanc reduction.- Bradsher reaction.- Brook rearrangement.- Brown hydroboration.- Bucherer carbazole synthesis.- Bucherer reaction.- Bucherer-Bergs reaction.- Buchner ring expansion.- Buchwald-Hartwig amination.- Burgess reagent.- Burke boronates.- Cadiot-Chodkiewicz coupling.- Camps quinoline synthesis.- Cannizzaro reaction.- Carroll rearrangement.- Castro-Stephens coupling.- Chan alkyne reduction.- Chan-Lam C-X coupling reaction.- Chapman rearrangement.- Chichibabin pyridine synthesis.- Chugaev elimination.- Ciamician-Dennsted rearrangement.- Claisen condensation.- Claisen isoxazole synthesis.- Claisen rearrangements.- Clemmensen reduction.- Combes quinoline synthesis.- Conrad-Limpach reaction.- Cope elimination reaction.- Cope rearrangement.- Corey-Bakshi-Shibata (CBS) reagent.- Corey-Chaykovsky reaction.- Corey-Fuchs reaction.- Corey-Kim oxidation.- Corey-Nicolaou macrolactonization.- Corey-Seebach reaction.- Corey-Winter olefin synthesis.- Criegee glycol cleavage.- Criegee mechanism of ozonolysis.- Curtius rearrangement.- Dakin oxidation.- Dakin-West reaction.- Darzens condensation.- Delepine amine synthesis.- de Mayo reaction.- Demjanov rearrangement.- Dess-Martin periodinane oxidation.- Dieckmann condensation.- Diels-Alder reaction.- Dienone-phenol rearrangement.- Di-Ï -methane rearrangement.- Doebner quinoline synthesis.- Doebner-von Miller reaction.- Dotz reaction.- Dowd-Beckwith ring expansion.- Dudley reagent.- Erlenmeyer-Plochl azlactone synthesis.- Eschenmoser's salt.- Eschenmoser-Tanabe fragmentation.- Eschweiler-Clarke reductive alkylation of amines.- Evans aldol reaction.- Favorskii rearrangement.- Feist-Benary furan synthesis.- Ferrier carbocyclization.- Ferrier glycal allylic rearrangement.- Fiesselmann thiophene synthesis.- Fischer indole synthesis.- Fischer oxazole synthesis.- Fleming-Kumada oxidation.- Friedel-Crafts reaction.- Friedlander quinoline synthesis.- Fries rearrangement.- Fukuyama amine synthesis.- Fukuyama reduction.- Gabriel synthesis.- Gabriel-Colman rearrangement.- Gassman indole synthesis.- Gattermann-Koch reaction.- Gewald aminothiophene synthesis.- Glaser coupling.- Gomberg-Bachmann reaction.- Gould-Jacobs reaction.- Grignard reaction.- Grob fragmentation.- Guareschi-Thorpe condensation.- Hajos-Wiechert reaction.- Haller-Bauer reaction.- Hantzsch dihydropyridine synthesis.- Hantzsch pyrrole synthesis.- Heck reaction.- Hegedus indole synthesis.- Hell-Volhard-Zelinsky reaction.- Henry nitroaldol reaction.- Hinsberg synthesis of thiophene derivatives.- Hiyama cross-coupling reaction.- Hofmann rearrangement.- Hofmann-Loffler-Freytag reaction.- Horner-Wadsworth-Emmons reaction.- Houben-Hoesch reaction.- Hunsdiecker-Borodin reaction.- Jacobsen-Katsuki epoxidation.- Japp-Klingemann hydrazone synthesis.- Jones oxidation.- Julia-Kocienski olefination.- Julia-Lythgoe olefination.- Kahne glycosidation.- Knoevenagel condensation.- Knorr pyrazole synthesis.- Koch-Haaf carbonylation.- Koenig-Knorr glycosidation.- Kostanecki reaction.- Krohnke pyridine synthesis.- Kumada cross-coupling reaction.- Lawesson's reagent.- Leuckart-Wallach reaction.- Lossen rearrangement.- McFadyen-Stevens reduction.- McMurry coupling.- Mannich reaction.- Martin's sulfurane dehydrating reagent.- Masamune-Roush conditions for the Horner-Emmons reaction.- Meerwein's salt.- Meerwein-Ponndorf-Verley reduction.- Meisenheimer complex.- [1,2]-Meisenheimer rearrangement.- [2,3]-Meisenheimer rearrangement.- Meyers oxazoline method.- Meyer-Schuster rearrangement.- Michael addition.- Michaelis-Arbuzov phosphonate synthesis.- Midland reduction.- Minisci reaction.- Mislow-Evans rearrangement.- Mitsunobu reaction.- Miyaura borylation.- Moffatt oxidation.- Morgan-Walls reaction.- Mori-Ban indole synthesis.- Mukaiyama aldol reaction.- Mukaiyama Michael addition.- Mukaiyama reagent.- Myers-Saito cyclization.- Nazarov cyclization.- Neber rearrangement.- Nef reaction.- Negishi cross-coupling reaction.- Nenitzescu indole synthesis.- Newman-Kwart rearrangement.- Nicholas reaction.- Nicolaou IBX dehydrogenation.- Noyori asymmetric hydrogenation.- Nozaki-Hiyama-Kishi reaction.- Nysted reagent.- Oppenauer oxidation.- Overman rearrangement.- Paal thiophene synthesis.- Paal-Knorr furan synthesis.- Paal-Knorr pyrrole synthesis.- Parham cyclization.- Passerini reaction.- Paterno-Buchi reaction.- Pauson-Khand reaction.- Payne rearrangement.- Pechmann coumarin synthesis.- Perkin reaction.- Petasis reaction.- Petasis reagent.- Peterson olefination.- Pictet-Gams isoquinoline synthesis.- Pictet-Spengler tetrahydroisoquinoline synthesis.- Pinacol rearrangement.- Pinner reaction.- Polonovski reaction.- Polonovski-Potier reaction.- Pomeranz-Fritsch reaction.- Prevost trans-dihydroxylation.- Prins reaction.- Pschorr cyclization.- Pummerer rearrangement.- Ramberg-Backlund reaction.- Reformatsky reaction.- Regitz diazo synthesis.- Reimer-Tiemann reaction.- Reissert reaction.- Reissert indole synthesis.- Ring-closing metathesis (RCM).- Ritter reaction.- Robinson annulation.- Robinson-Gabriel synthesis.- Robinson-Schopf reaction.- Rosenmund reduction.- Rubottom oxidation.- Rupe rearrangement.- Saegusa oxidation.- Sakurai allylation reaction.- Sandmeyer reaction.- Schiemann reaction.- Schmidt rearrangement.- Schmidt's trichloroacetimidate glycosidation reaction.- Shapiro reaction.- Sharpless asymmetric amino-hydroxylation.- Sharpless asymmetric dihydroxylation.- Sharpless asymmetric epoxidation.- Sharpless olefin synthesis.- Simmons-Smith reaction.- Skraup quinoline synthesis.- Smiles rearrangement.- Sommelet reaction.- Sommelet-Hauser rearrangement.- Sonogashira reaction.- Staudinger ketene cycloaddition.- Staudinger reduction.- Stetter reaction.- Still-Gennari phosphonate reaction.- Stille coupling.- Stille-Kelly reaction.- Stobbe condensation.- Strecker amino acid synthesis.- Suzuki-Miyaura coupling.- Swern oxidation.- Takai reaction.- Tebbe's reagent.- TEMPO oxidation.- Thorpe-Ziegler reaction.- Tsuji-Trost reaction.- Ugi reaction.- Ullmann coupling.- van Leusen oxazole synthesis.- Vilsmeier- Haack reaction.- Vinylcyclopropane-cyclopentene rearrangement.- von Braun reaction.- Wacker oxidation.- Wagner-Meerwein rearrangement.- Weiss-Cook reaction.- Wharton reaction.- White Reagent.- Willgerodt-Kindler reaction.- Wittig reaction.- [1,2]-Wittig rearrangement.- [2,3]-Wittig rearrangement.- Wohl-Ziegler reaction.- Wolff rearrangement.- Wolff-Kishner reduction.- Woodward cis-dihydroxylation.- Yamaguchi esterification.- Zincke reaction.
Responsibility: Jie Jack Lie.

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