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09677nam a22003615i 4500 |
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978-3-642-01053-8 |
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20191026031759.0 |
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cr nn 008mamaa |
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100316s2009 gw | s |||| 0|eng d |
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|a 9783642010538
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|a 10.1007/978-3-642-01053-8
|2 doi
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|a Sistema de Bibliotecas del Tecnológico de Costa Rica
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|a Li, Jie Jack.
|e author.
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|a Name Reactions
|b A Collection of Detailed Mechanisms and Synthetic Applications /
|c by Jie Jack Li.
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|a 4th ed. 2009.
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|a Berlin, Heidelberg :
|b Springer Berlin Heidelberg :
|b Imprint: Springer,
|c 2009.
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|a XXII, 621 p. 6 illus.
|b online resource.
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|a text
|b txt
|2 rdacontent
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|a computer
|b c
|2 rdamedia
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|a online resource
|b cr
|2 rdacarrier
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|a Alder ene reaction -- Aldol condensation -- Algar#x2014; Flynn#x2014; Oyamada Reaction -- Allan#x2013;Robinson reaction -- Arndt#x2014;Eistert homologation -- Baeyer#x2013;Villiger oxidation -- Baker#x2013;Venkataraman rearrangement -- Bamford#x2013;Stevens reaction -- Barbier coupling reaction -- Bartoli indole synthesis -- Barton radical decarboxylation -- Barton#x2013;McCombie deoxygenation -- Barton nitrite photolysis -- Batcho#x2013;Leimgruber indole synthesis -- Baylis#x2013;Hillman reaction -- Beckmann rearrangement -- Benzilic acid rearrangement -- Benzoin condensation -- Bergman cyclization -- Biginelli pyrimidone synthesis -- Birch reduction -- Bischler#x2013;M#x00F6;hlau indole synthesis -- Bischler#x2013;Napieralski reaction -- Blaise reaction -- Blum#x2013;Ittah aziridine synthesis -- Boekelheide reaction -- Boger pyridine synthesis -- Borch reductive amination -- Borsche#x2013;Drechsel cyclizations -- Boulton#x2013;Katritzky rearrangement -- Bouveault aldehyde synthesis -- Bouveault#x2014;Blanc reduction -- Bradsher reaction -- Brook rearrangement -- Brown hydroboration -- Bucherer carbazole synthesis -- Bucherer reaction -- Bucherer#x2014;Bergs reaction -- B#x00FC;chner ring expansion -- Buchwald#x2013;Hartwig amination -- Burgess reagent -- Burke boronates -- Cadiot#x2013;Chodkiewicz coupling -- Camps quinoline synthesis -- Cannizzaro reaction -- Carroll rearrangement -- Castro#x2013;Stephens coupling -- Chan alkyne reduction -- Chan#x2013;Lam C#x2013;X coupling reaction -- Chapman rearrangement -- Chichibabin pyridine synthesis -- Chugaev elimination -- Ciamician#x2013;Dennsted rearrangement -- Claisen condensation -- Claisen isoxazole synthesis -- Claisen rearrangements -- Clemmensen reduction -- Combes quinoline synthesis -- Conrad#x2013;Limpach reaction -- Cope elimination reaction -- Cope rearrangement -- Corey#x2013;Bakshi#x2013;Shibata (CBS) reagent -- Corey#x2013;Chaykovsky reaction -- Corey#x2013;Fuchs reaction -- Corey#x2013;Kim oxidation -- Corey#x2013;Nicolaou macrolactonization -- Corey#x2013;Seebach reaction -- Corey#x2013;Winter olefin synthesis -- Criegee glycol cleavage -- Criegee mechanism of ozonolysis -- Curtius rearrangement -- Dakin oxidation -- Dakin#x2013;West reaction -- Darzens condensation -- Del#x00E9;pine amine synthesis -- de Mayo reaction -- Demjanov rearrangement -- Dess#x2013;Martin periodinane oxidation -- Dieckmann condensation -- Diels#x2013;Alder reaction -- Dienone#x2013;phenol rearrangement -- Di#x2013;#x03C0;#x2013;methane rearrangement -- Doebner quinoline synthesis -- Doebner#x2013;von Miller reaction -- D#x00F6;tz reaction -- Dowd#x2013;Beckwith ring expansion -- Dudley reagent -- Erlenmeyer#x2013;Pl#x00F6;chl azlactone synthesis -- Eschenmoser#x2019;s salt -- Eschenmoser#x2013;Tanabe fragmentation -- Eschweiler#x2013;Clarke reductive alkylation of amines -- Evans aldol reaction -- Favorskii rearrangement -- Feist#x2013;B#x00E9;nary furan synthesis -- Ferrier carbocyclization -- Ferrier glycal allylic rearrangement -- Fiesselmann thiophene synthesis -- Fischer indole synthesis -- Fischer oxazole synthesis -- Fleming#x2013;Kumada oxidation -- Friedel#x2013;Crafts reaction -- Friedl#x00E4;nder quinoline synthesis -- Fries rearrangement -- Fukuyama amine synthesis -- Fukuyama reduction -- Gabriel synthesis -- Gabriel#x2013;Colman rearrangement -- Gassman indole synthesis -- Gattermann#x2013;Koch reaction -- Gewald aminothiophene synthesis -- Glaser coupling -- Gomberg#x2013;Bachmann reaction -- Gould#x2013;Jacobs reaction -- Grignard reaction -- Grob fragmentation -- Guareschi#x2013;Thorpe condensation -- Hajos#x2013;Wiechert reaction -- Haller#x2013;Bauer reaction -- Hantzsch dihydropyridine synthesis -- Hantzsch pyrrole synthesis -- Heck reaction -- Hegedus indole synthesis -- Hell#x2014;Volhard#x2014;Zelinsky reaction -- Henry nitroaldol reaction -- Hinsberg synthesis of thiophene derivatives -- Hiyama cross-coupling reaction -- Hofmann rearrangement -- Hofmann#x2013;L#x00F6;ffler#x2013;Freytag reaction -- Horner#x2014;Wadsworth#x2014;Emmons reaction -- Houben#x2013;Hoesch reaction -- Hunsdiecker#x2013;Borodin reaction -- Jacobsen#x2013;Katsuki epoxidation -- Japp#x2013;Klingemann hydrazone synthesis -- Jones oxidation -- Julia#x2013;Kocienski olefination -- Julia#x2013;Lythgoe olefination -- Kahne glycosidation -- Knoevenagel condensation -- Knorr pyrazole synthesis -- Koch#x2013;Haaf carbonylation -- Koenig#x2013;Knorr glycosidation -- Kostanecki reaction -- Kr#x000F6;hnke pyridine synthesis -- Kumada cross-coupling reaction -- Lawesson#x2019;s reagent -- Leuckart#x2013;Wallach reaction -- Lossen rearrangement -- McFadyen#x2013;Stevens reduction -- McMurry coupling -- Mannich reaction -- Martin#x2019;s sulfurane dehydrating reagent -- Masamune#x2013;Roush conditions for the Horner#x2013;Emmons reaction -- Meerwein#x2019;s salt -- Meerwein#x2013;Ponndorf#x2013;Verley reduction -- Meisenheimer complex -- [1,2]-Meisenheimer rearrangement -- [2,3]-Meisenheimer rearrangement -- Meyers oxazoline method -- Meyer#x2013;Schuster rearrangement -- Michael addition -- Michaelis#x2013;Arbuzov phosphonate synthesis -- Midland reduction -- Minisci reaction -- Mislow#x2013;Evans rearrangement -- Mitsunobu reaction -- Miyaura borylation -- Moffatt oxidation -- Morgan#x2013;Walls reaction -- Mori#x2013;Ban indole synthesis -- Mukaiyama aldol reaction -- Mukaiyama Michael addition -- Mukaiyama reagent -- Myers#x2013;Saito cyclization -- Nazarov cyclization -- Neber rearrangement -- Nef reaction -- Negishi cross-coupling reaction -- Nenitzescu indole synthesis -- Newman#x2013;Kwart rearrangement -- Nicholas reaction -- Nicolaou IBX dehydrogenation -- Noyori asymmetric hydrogenation -- Nozaki#x2013;Hiyama#x2013;Kishi reaction -- Nysted reagent -- Oppenauer oxidation -- Overman rearrangement -- Paal thiophene synthesis -- Paal#x2013;Knorr furan synthesis -- Paal#x2013;Knorr pyrrole synthesis -- Parham cyclization -- Passerini reaction -- Patern#x00F3;#x2013;B#x00FC;chi reaction -- Pauson#x2013;Khand reaction -- Payne rearrangement -- Pechmann coumarin synthesis -- Perkin reaction -- Petasis reaction -- Petasis reagent -- Peterson olefination -- Pictet#x2013;Gams isoquinoline synthesis -- Pictet#x2013;Spengler tetrahydroisoquinoline synthesis -- Pinacol rearrangement -- Pinner reaction -- Polonovski reaction -- Polonovski#x2013;Potier reaction -- Pomeranz#x2013;Fritsch reaction -- Pr#x00E9;vost trans-dihydroxylation -- Prins reaction -- Pschorr cyclization -- Pummerer rearrangement -- Ramberg#x2013;B#x00E4;cklund reaction -- Reformatsky reaction -- Regitz diazo synthesis -- Reimer#x2013;Tiemann reaction -- Reissert reaction -- Reissert indole synthesis -- Ring-closing metathesis (RCM) -- Ritter reaction -- Robinson annulation -- Robinson#x2013;Gabriel synthesis -- Robinson#x2013;Sch#x00F6;pf reaction -- Rosenmund reduction -- Rubottom oxidation -- Rupe rearrangement -- Saegusa oxidation -- Sakurai allylation reaction -- Sandmeyer reaction -- Schiemann reaction -- Schmidt rearrangement -- Schmidt#x2019;s trichloroacetimidate glycosidation reaction -- Shapiro reaction -- Sharpless asymmetric amino-hydroxylation -- Sharpless asymmetric dihydroxylation -- Sharpless asymmetric epoxidation -- Sharpless olefin synthesis -- Simmons#x2013;Smith reaction -- Skraup quinoline synthesis -- Smiles rearrangement -- Sommelet reaction -- Sommelet#x2013;Hauser rearrangement -- Sonogashira reaction -- Staudinger ketene cycloaddition -- Staudinger reduction -- Stetter reaction -- Still#x2013;Gennari phosphonate reaction -- Stille coupling -- Stille#x2013;Kelly reaction -- Stobbe condensation -- Strecker amino acid synthesis -- Suzuki#x2013;Miyaura coupling -- Swern oxidation -- Takai reaction -- Tebbe#x2019;s reagent -- TEMPO oxidation -- Thorpe#x2013;Ziegler reaction -- Tsuji#x2013;Trost reaction -- Ugi reaction -- Ullmann coupling -- van Leusen oxazole synthesis -- Vilsmeier#x2013; Haack reaction --
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|a Vinylcyclopropane#x2013;cyclopentene rearrangement -- von Braun reaction -- Wacker oxidation -- Wagner#x2013;Meerwein rearrangement -- Weiss#x2013;Cook reaction -- Wharton reaction -- White Reagent -- Willgerodt#x2013;Kindler reaction -- Wittig reaction -- [1,2]-Wittig rearrangement -- [2,3]-Wittig rearrangement -- Wohl#x2013;Ziegler reaction -- Wolff rearrangement -- Wolff#x2013;Kishner reduction -- Woodward cis-dihydroxylation -- Yamaguchi esterification -- Zincke reaction.
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| 650 |
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|a Organic chemistry.
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| 650 |
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|a Inorganic chemistry.
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| 650 |
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|a Biochemistry.
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|a Medicinal chemistry.
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|a Organic Chemistry.
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|a Inorganic Chemistry.
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| 650 |
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|a Biochemistry, general.
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| 650 |
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|a Medicinal Chemistry.
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|a SpringerLink (Online service)
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|t Springer eBooks
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|u https://doi.org/10.1007/978-3-642-01053-8
|