Inhaltsangabe
Abnormal Claisen rearrangement.- Alder ene reaction.- Allan-Robinson reaction.- Alper carbonylation.- Amadori glucosamine rearrangement.- Angeli-Rimini hydroxamic acid synthesis.- ANRORC mechanism.- Arndt-Eistert homologation.- Baeyer-Drewson indigo synthesis.- Baeyer-Villiger oxidation.- Baker-Venkataraman rearrangement.- Bamberger rearrangement.- Bamford-Stevens reaction.- Bargellini reaction.- Bartoli indole synthesis.- Barton decarboxylation reaction.- Barton-McCombie deoxygenation reaction.- Barton nitrite photolysis.- Baylis-Hillman reaction.- 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.- Blanc chloromethylation reaction.- Boekelheide reaction.- Boger pyridine synthesis.- Boord reaction.- Borsche-Drechsel cyclization.- Boulton-Katritzky rearrangement.- Bouveault aldehyde synthesis.- Bouveault-Blanc reduction.- Boyland-Sims oxidation.- Bradsher reaction.- Brook rearrangement.- Brown hydroboration reaction.- Bucherer carbazole synthesis.- Bucherer reaction.- Bucherer-Bergs reaction.- Buchner-Curtius-Schlotterbeck reaction.- Buchner method of ring expansion.- Buchwald-Hartwig C-N bond and C-O bond formation reactions.- Burgess dehydrating reagent.- Cadiot-Chodkiewicz coupling.- Cannizzaro disproportionation reaction.- Carroll rearrangement.- Castro-Stephens coupling.- Chapman rearrangement.- Chichibabin amination reaction.- Chichibabin pyridine synthesis.- Chugaev elimination.- Ciamician-Dennsted rearrangement.- Claisen, Eschenmoser-Claisen, Johnson-Claisen, and Ireland-Claisen rearrangements.- Clark-Eschweiler reductive alkylation of amines.- Combes quinoline synthesis.- Conrad-Lipach reaction.- Cope elimination reaction.- Cope, oxy-Cope, and anionic oxy-Cope rearrangements.- Corey-Chaykovsky epoxidation.- Corey-Fuchs reaction.- Corey-Bakshi-Shibata (CBS) reduction.- Corey-Kim oxidation.- Corey-Winter olefin synthesis.- Cornforth rearrangement.- Criegee glycol cleavage.- Criegee mechanism of ozonolysis.- Curtius rearrangement.- Dakin reaction.- Dakin-West reaction.- Danheiser annulation.- Darzens glycidic ester condensation.- Davis chiral oxaziridine reagents.- de Mayo reaction.- Demjanov rearrangement.- Dess-Martin periodinane oxidation.- Dieckmann condensation.- Diels-Alder reaction, inverse electronic demand Diels-Alder reaction, hetero-Diels-Alder reaction.- Dienone-phenol rearrangement.- Di-?-methane rearrangement.- Doebner reaction.- Doebner-von Miller reaction.- Doering-LaFlamme allene synthesis.- Dornow-Wiehler isoxazole synthesis.- Dötz reaction.- Dutt-Wormall reaction.- Eschenmoser coupling reaction.- Eschenmoser-Tanabe fragmentation.- Étard reaction.- Evans aldol reaction.- Favorskii rearrangement and Quasi-Favorskii rearrangement.- Feist-Bénary furan synthesis.- Ferrier rearrangement.- Fischer-Hepp rearrangement.- Fischer indole synthesis.- Fischer-Speier esterification.- Fleming oxidation.- Forster reaction.- Frater-Seebach alkylation.- Friedel-Crafts reaction.- Friedländer synthesis.- Fries rearrangement.- Fritsch-Buttenberg-Wiechell rearrangement.- Fujimoto-Belleau reaction.- Fukuyama amine synthesis.- Gabriel synthesis.- Gassman indole synthesis.- Gattermann-Koch reaction.- Gewald aminothiophene synthesis.- Glaser coupling.- Gomberg-Bachmann reaction.- Gribble indole reduction.- Gribble reduction of diaryl ketones.- Grob fragmentation.- Guareschi-Thorpe condensation.- Hajos-Wiechert reaction.- Haller-Bauer reaction.- Hantzsch pyridine synthesis.- Hantzsch pyrrole synthesis.- Haworth reaction.- Hayashi rearrangement.- Heck reaction.- Hegedus indole synthesis.- Hell-Volhardt-Zelinsky reaction.- Henry reaction (nitroaldol reaction).- Herz reaction.- Heteroaryl Heck reaction.- Hiyama cross-coupling reaction.- Hodges-Vedejs metallation of oxazoles.- Hofmann rearrangement (Hofmann degradation reaction).-
Die Inhaltsangabe kann sich auf eine andere Ausgabe dieses Titels beziehen.
