Name Reactions A Collection of Detailed Mechanisms and Synthetic Applications /
| Autor principal: | |
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| Autor Corporativo: | |
| Formato: | eBook |
| Lenguaje: | English |
| Publicado: |
Berlin, Heidelberg :
Springer Berlin Heidelberg : Imprint: Springer,
2009.
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| Edición: | 4th ed. 2009. |
| Materias: | |
| Acceso en línea: | https://doi.org/10.1007/978-3-642-01053-8 |
Tabla de Contenidos:
- 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
- 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.