includes index

Alder ene reaction;Aldol condensation;Algar-Flynn-Oyamada Reaction;Allan-Robinson reaction;Appel reaction;Arndt-Eistert homologation;Baeyer-Villiger oxidation;Baker-Venkataraman rearrangement;Bamberger rearrangement;Bamford-Stevens reaction;Barbier coupling 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;Beirut reaction;Benzilic acid rearrangement;Benzoin condensation;Bergman cyclization;Biginelli pyrimidone synthesis;Birch reduction;Bischler-Moehlau indole synthesis;Bischler-Napieralski reaction;Blaise reaction;Blanc chloromethylation;Blum aziridine synthesis;Boekelheide reaction;Boger pyridine synthesis;Borch reductive amination;Borsche-Drechsel cyclization;Boulton-Katritzky rearrangement;Bouveault aldehyde synthesis;Bouveault-Blanc reduction;Boyland-Sims oxidation;Bradsher reaction;Brook rearrangement;Brown hydroboration;Bucherer carbazole synthesis;Bucherer reaction;Bucherer-Bergs reaction;Buchner-Curtius-Schlotterbeck reaction;Buchner method of ring expansion;Buchwald-Hartwig C-N and C-O bond formation reactions;Burgess dehydrating reagent;Cadiot-Chodkiewicz coupling;Camps quinolinol synthesis;Cannizzaro disproportionation;Carroll rearrangement;Castro-Stephens coupling;Chan alkyne reduction;Chan-Lam 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) reduction;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 glycidic ester condensation;Davis chiral oxaziridine reagents;Delepine amine synthesis;de Mayo reaction;Demjanov rearrangement;Dess-Martin periodinane oxidation;Dieckmann condensation;Diels-Alder reaction;Dienone-phenol rearrangement;Di-?-methane rearrangement;Doebner quinoline synthesis;Doetz reaction;Dowd-Beckwith ring expansion;Erlenmeyer-Ploechl azlactone synthesis;Eschenmoser-Tanabe fragmentation;Eschweiler-Clarke reductive alkylation of amines;Evans aldol reaction;Favorskii rearrangement and quasi-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-Loeffler-Freytag reaction;Horner-Wadsworth-Emmons reaction;Houben-Hoesch reaction;Hunsdiecker-Borodin reaction;Hurd-Mori 1,2,3-thiadiazole synthesis;Jacobsen-Katsuki epoxidation;Japp-Klingemann hydrazone synthesis;Jones oxidation;Julia-Kocienski olefination;Julia-Lythgoe olefination;Kahne-Crich glycosidation;Keck macrolactonization;Knoevenagel condensation;Knorr pyrazole synthesis;Koch-Haaf carbonylation;Koenig-Knorr glycosidation;Kolbe-Schmitt reaction;Kostanecki reaction;Kroehnke pyridine synthesis;Kumada cross-coupling reaction;Lawesson's reagent;Leuckart-Wallach reaction;Lossen rearrangement;McFadyen-Stevens reduction;McMurry coupling;MacMillan catalyst;Mannich reaction;Marshall boronate fragmentation;Martin's sulfurane dehydrating reagent;Masamune-Roush conditions;Meerwein-Ponndorf-Verley reduction;Meisenheimer complex;[1,2]-Meisenheimer rearrangement;[2,3]-Meisenheimer rearrangement;Meth-Cohn quinoline synthesis;Meyers oxazoline method;Meyer-Schuster rearrangement;Michael addition;Michaelis-Arbuzov phosphonate synthesis;Midland reduction;Mislow-Evans rearrangement;Mitsunobu reaction;Miyaura borylation;Moffatt oxidation;Montgomery coupling;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;Nicholas reaction;Nicolaou dehydrogenation;Nicolaou hydroxy-dithioketal cyclization;Nicolaou hydroxy-ketone reductive cyclic ether formation;Nicolaou oxyselenation;Noyori asymmetric hydrogenation;Nozaki-Hiyama-Kishi reaction;Oppenauer oxidation;Overman rearrangement;Paal thiophene synthesis;Paal-Knorr furan synthesis;Parham cyclization;Passerini reaction;Paterno-Buchi reaction;Pauson-Khand cyclopentenone synthesis;Payne rearrangement;Pechmann coumarin synthesis;Perkin reaction;Petasis reaction;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 aldehyde synthesis;Reissert indole synthesis;Ring-closing metathesis (RCM);Ritter reaction;Robinson annulation;Robinson-Gabriel synthesis;Robinson-Schoepf reaction;Rosenmund reduction;Rubottom oxidation;Rupe rearrangement;Saegusa oxidation;Sakurai allylation reaction;Sandmeyer reaction;Schiemann reaction;Schmidt reaction;Schmidt's trichloroacetimidate glycosidation reaction;Shapiro reaction;Sharpless asymmetric amino hydroxylation;Sharpless asymmetric epoxidation;Sharpless asymmetric dihydroxylation;Sharpless olefin synthesis;Simmons-Smith reaction;Skraup quinoline synthesis;Smiles rearrangement;Sommelet reaction;Sommelet-Hauser rearrangement;Sonogashira reaction;Staudinger ketene cycloaddition;Staudinger reduction;Sternbach benzodiazepine synthesis;Stetter reaction;Still-Gennari phosphonate reaction;Stille coupling;Stille-Kelly reaction;Stobbe condensation;Stork enamine reaction;Strecker amino acid synthesis;Suzuki coupling;Swern oxidation;Takai iodoalkene synthesis;Tebbe olefination;TEMPO-mediated oxidation;Thorpe-Ziegler reaction;Tsuji-Trost reaction;Ugi reaction;Ullmann reaction;van Leusen oxazole synthesis;Vilsmeier-Haack reaction;Vilsmeier mechanism for acid chloride formation;Vinylcyclopropane-cyclopentene rearrangement;von Braun reaction;Wacker oxidation;Wagner-Meerwein rearrangement;Weiss-Cook reaction;Wharton oxygen transposition reaction;Willgerodt-Kindler reaction;Wittig reaction;[1,2]-Wittig rearrangement;[2,3]-Wittig rearrangement;Wohl-Ziegler reaction;Wolff rearrangement;Wolff-Kishner reduction;Yamaguchi esterification;Zincke reaction.