Title Name reactions : a collection of detailed mechanisms and synthetic applications / Jie Jack Li

Edition Fifth edition Published Cham : Springer, 2014

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Description 1 online resource (xxii, 681 pages) : illustrations (some color) Contents Preface -- Abbreviations and acronyms -- Alder ene reaction -- Aldol condensation -- Algar-Flynn-Oyamada reaction -- Allan-Robinson reaction -- Arndt-Eistert homologation -- Baeyer-Villiger oxidation -- Baker-Venkataraman rearrangement -- Bamford-Stevens reaction -- Baran reagents -- Barbier reaction -- Bargellini reaction -- Bartoli indole synthesis -- Barton radical decarboxylation -- Barton-McCombie deoxygenation -- Barton nitrite photolysis -- Barton-Zard reaction -- Batcho-Leimgruber indole synthesis -- Baylis-Hillman reaction -- Beckmann rearrangement. Abnormal Beckmann rearrangement -- Beirut reaction -- Benzilic acid rearrangement -- Benzoin condensation -- Bergman cyclization -- Biginelli pyrimidone synthesis -- Birch reduction -- Bischler-Möhlau 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 -- Boyland-Sims oxidation. Elbs oxidation -- Bradsher reaction -- Brook rearrangement -- Brown hydroboration -- Bucherer carbazole synthesis -- Bucherer reaction -- Bucherer-Bergs reaction -- Büchner ring expansion -- Buchwald-Hartwig amination -- Burgess reagent -- Burke boronates -- Cadiot-Chodkiewicz coupling -- Cadogan-Sundberg indole synthesis -- Camps quinoline synthesis -- Cannizzaro reaction -- Carroll rearrangement -- Castro-Stephens coupling -- C-H activation. Catellani reaction. Sanford reaction. White catalyst. Yu C-H activation -- 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. para-Claisen rearrangement. Abnormal Claisen rearrangement. Eschenmoser-Claisen (silyl ketene acetal) rearrangement. Johnson-Claisen (orthoester) rearrangement -- Clemmensen reduction -- Combes quinoline synthesis -- Conrad-Limpach reaction -- Cope elimination reaction -- Cope rearrangement. Anionic Cope rearrangement. Oxy-Cope rearrangement. Siloxy-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 -- Danheiser annulation -- Darzens condensation -- Delépine amine synthesis -- de Mayo reaction -- Demjanov rearrangement. Tiffenau-Demjanov rearrangement -- Dess-Martin periodinane oxidation -- Dieckmann condensation -- Diels-Alder reaction. Inverse electronic demand Diels-Alder reaction. Heter-Diels-Alder reaction -- Dienone-phenol rearrangement -- Doebner quinoline synthesis -- Doebner-von Miller reaction -- Dötz reaction -- Dowd-Beckwith ring expansion -- Dudley reagent -- Erlenmeyer-Plöchl azlactone synthesis -- Eschenmoser's salt -- Eschenmoser-Tanabe fragmentation -- Eschweiler-Clarke reductive alkylation of amines -- Evans aldol reaction -- Favorskii rearrangement. Quasi-Favorskii rearrangement -- Feist-Bénary furan synthesis -- Ferrier carbocyclization -- Ferrier glycal allylic rearrangement -- Fiesselmann thiophene synthesis -- Fischer-Speier estrification -- Fischer indole synthesis -- Fischer oxazole synthesis -- Fleming-Kumada oxidation. Tamao-Kumada oxidation -- Friedel-Crafts reaction. Friedel-Crafts acylation reaction. Friedel-Crafts alkylation reaction -- Friedländer quinoline synthesis -- Fries rearrangement -- Fukuyama amine synthesis -- Fukuyama reduction -- Gabriel synthesis. Ing-Manske procedure -- Gabriel-Colman rearrangement -- Gassman indole synthesis -- Gattermann-Koch reaction -- Gewald aminothiophene synthesis -- Glaser coupling. Eglinton 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. Heteroaryl Heck reaction -- Hegedus indole synthesis -- Hell-Volhard-Zelinsky reaction -- Henry nitroaldol reaction -- Hinsberg synthesis of thiophenes -- Hiyama cross-coupling reaction -- Hofmann elimination -- Hofmann rearrangement -- Hofmann-Löffler-Freytag reaction -- Horner-Wadsworth-Emmons reaction -- Houben-Hoesch reaction -- Hunsdiecker-Borodin reaction -- Jacobsen-Katsuki epoxidation -- Japp-Klingemann hydrazone synthesis -- Jones oxidation. Collins oxidation. PCC oxidation. PDC oxidation -- Julia-Kocienski olefination -- Julia-Lythgoe olefination -- Kahne glycosidation -- Knoevenagel condensation -- Knorr pyrazole synthesis -- Koch-Haaf carbonylation -- Koenig-Knorr glycosidation -- Kostanecki reaction -- Kröhnke pyridine synthesis -- Krapcho reaction -- Kumada cross-coupling reaction -- Lawesson's reagent -- Leuckart-Wallach reaction -- Li A³ reaction -- Lossen rearrangement -- McFadyen-Stevens reduction -- McMurry coupling -- MacMillan catalyst -- Mannich reaction -- Markovnikov's rule. Anti-Markovnikov -- 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. Pictet-Huber 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 -- Paternó-Büchi reaction -- Pauson-Khand reaction -- Payne rearrangement -- Pechmann coumarin synthesis -- Perkin reaction -- Perkow vinyl phosphate synthesis -- 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. Schlittler-Müller modification -- Prévost trans-dihydroxylation -- Prins reaction -- Pschorr cyclization -- Pummerer rearrangement -- Ramberg-Bäcklund 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-Schöpf reaction -- Rosenmund reduction -- Rubottom oxidation -- Rupe rearrangement -- Saegusa oxidation -- Sakurai allylation reaction -- Sandmeyer reaction -- Schiemann reaction -- Schmidt rearrangement -- Schmidt's trichloroacetimidate glycosidation reaction -- Scholl reaction -- Shapiro reaction -- Sharpless asymmetric amino-hydroxylation -- Sharpless asymmetric dihydroxylation -- Sharpless asymmetric epoxidation -- Sharpless olefin synthesis -- Shi asymmetric epoxidation -- Simmons-Smith reaction -- Skraup quinoline synthesis -- Smiles rearrangement. Truce-Smile rearrangement -- Sommelet reaction -- Sommelet-Hauser rearrangement -- Sonogashira reaction -- Staudinger ketene cycloaddition -- Staudinger reduction -- Stetter reaction -- Stevens rearrangement -- Still-Gennari phosphonate reaction -- Stille coupling -- Stille-Kelly reaction -- Stobbe condensation -- Stork-Danheiser transposition -- 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 -- Williamson ether synthesis -- Willgerodt-Kindler reaction -- Wittig reaction. Schlosser modification of the Wittig reaction -- [1,2]-Wittig rearrangement -- [2,3]-Wittig rearrangement -- Wohl-Ziegler reaction -- Wolff rearrangement -- Wolff-Kishner reduction -- Woodward cis-dihydroxylation -- Yamaguchi esterification -- Zaitsev's elimination rule -- Zhang enyne cycloisomerization -- Zimmerman rearrangement -- Zincke reaction -- Zinin benzidine (semidne) rearrangement -- Index Summary In this fifth edition of Jack Jie Li's seminal "Name Reactions", the author has added twenty-seven new name reactions to reflect the recent advances in organic chemistry. As in previous editions, each reaction is delineated by its detailed step-by-step, electron-pushing mechanism and supplemented with the original and the latest references, especially from review articles. Now with addition of many synthetic applications, this book is not only an indispensable resource for advanced undergraduate and graduate students, but is also a good reference book for all organic chemists in both industry and academia. Unlike other books on name reactions in organic chemistry, Name Reactions, A Collection of Detailed Reaction Mechanisms and Synthetic Applications focuses on the reaction mechanisms. It covers over 320 classical as well as contemporary name reactions Analysis chemie chemistry organische scheikunde organic chemistry biochemie biochemistry anorganische scheikunde inorganic chemistry Chemistry (General) Chemie (algemeen) Notes Includes index Online resource; title from PDF title page (SpringerLink, viewed February 3, 2014) Subject Chemical reactions. Chemistry, Organic. organic chemistry. Chimie. Science des matériaux. Chemical reactions Chemistry, Organic Form Electronic book ISBN 9783319039794 3319039792 3319039784 9783319039787

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