Asymmetric synthesis. CBS reduction ; Davis chiral oxaziridine reagents ; Midland reduction ; Noyori catalytic asymmetric hydrogenation ; Sharpless asymmetric hydroxylation reactions Reduction. Eschweiler-Clark reductive alkylation of amines ; Gribble reduction of diaryl ketones ; Luche reduction ; Meerwein-Ponndorf-Verley reduction ; Staudinger reaction ; Wharton reaction Oxidation. Baeyer-Villiger oxidation ; Brown hydroboration reaction ; Burgess dehydrating reagent ; Corey-Kim oxidation ; Dess-Martin periodinane oxidation ; Tamao-Kumada-Fleming oxidation ; Martin's sulfurane dehydrating reagent ; Oppenauer oxidation ; Prilezhaev reaction ; Rubottom oxidation ; Swern oxidation ; Wacker-Tsuji oxidation ; Woodward cis-dihydroxylation
Olefination. Chugaev elimination ; Cope elimination reaction ; Corey-Winter olefin synthesis ; Perkin reaction (cinnamic acid synthesis) ; Perkow vinyl phosphate synthesis ; Ramberg-Bäcklund olefin synthesis ; Shapiro reaction ; Zaitsev elimination
Amine synthesis. Fukuyama amine synthesis ; Gabriel synthesis ; Leuckart-Wallach reaction
Carboxylic acid derivatives synthesis. Fischer-Speier esterification ; Mukaiyama esterification ; Ritter reaction ; Strecker amino acid synthesis ; Yamada coupling reagent ; Yamaguchi esterification
Miscellaneous functional group manipulations. Balz-Schiemann reaction ; Buchwald-Hartwig reactions ; Haloform reaction ; Hunsdiecker reaction ; Japp-Klingemann hydrazone synthesis ; Krapcho decarboxylation ; Nef reaction ; Prins reaction ; Regitz diazo synthesis ; Sommelet reaction.
