Chiral auxiliaries and catalysts

This article has no abstract. Keywords: small ring synthesis; 1,3-dipolar cycloadditions; Diels–Alder reactions; oxidations; dihydroxylation; homogeneous hydrogenation; reductions with borane; α-cyanohydrination; transpositional reduction of allylic carbonates; addition of R2Zn to aldehydes; other organometallic additions; aldolization and related reactions; Michael reaction; proton transfer; acylation; addition to double bonds; Heck reactions; Aldol reactions; substitutions; alkylations; Michael additions; organometallic reactions; cyanohydrination and strecker synthesis; formation of three-membered rings; cycloadditions; Pauson–Khand reaction; epoxidation; oxidation of sulfides; allylic oxidations; reduction of ketones with borane; reduction with complex metal hydrides; reduction with hydrosilanes; asymmetric hydrogenation; Ireland–Claisen rearrangement; recovery of auxiliaries; kinetic resolutions; enolization and protonation; alkylations; α-heterofunctionalizations; displacements involving allylic systems; opening of epoxides; addition to C = O; addition to C = N; addition of allylmetals to C = X; addition to C = C; Michael reactions; cycloadditions; asymmetric hydrogenation; ketone reduction by hydrogen transfer; reduction using complex metal hydrides; reduction using boranes; reduction using hydrosilanes; oxidations; epoxidations; condensation with carbonyl compounds; cyclopropanation; Aldol reactions; rearrangements; other enantioselective reactions; chiral derivatizing agents; kinetic resolutions; halogenations; alkylations; displacements involving allylic systems; opening of epoxides and aziridines; addition to CO; addition to CN; addition to CC; Michael reactions; cycloadditions; epoxidations; ketone reductions; asymmetric hydrogenation; other enantioselective reactions; reagent preparations; kinetic resolutions; halogenation; alkylations; displacements involving allylic systems; opening of epoxides; addition to C = O; addition to C = N; addition to multiple CC bonds; epoxidation and aziridination reactions; Michael reactions; cycloadditions; ketone reductions; asymmetric hydrogenation; oxidations; other enantioselective reactions; resolutions; halogenation; alkylations and acylations; allylic substitutions; addition to CO bond; addition to CN bond; conjugate additions; addition to CC bond; cycloadditions; coupling reactions; epoxidation and dihydroxylation reactions; oxidations; reduction and hydrogenation; other enantioselective reactions; resolution and racemization; electrophilic substitution; alkylations and acylations; allylic substitutions; opening of small heterocycles; addition to CO bond; addition to CN bond; conjugate additions; addition to unactivated CC bond; cycloadditions; epoxidation and other oxidation reactions; hydrogenation and reduction; isomerization and rearrangements; other enantioselective reactions; kinetic resolution; desymmetrization; electrophilic substitution; allylic substitutions; addition to CO bond; addition to CN bond; conjugate additions; cycloadditions; epoxidation and other oxidation reactions; hydrogenation and reduction of CC bonds; hydrogenation and reduction of CO bond; hydrogenation and reduction of CN bond; isomerization and rearrangements; insertion reactions; coupling reactions; kinetic resolution and desymmetrizaion; electrophilic substitution; allylic substitutions; addition to CO bond; addition to CN bond; conjugate additions; cycloadditions; addition to CC bonds; coupling reactions; epoxidation and other oxidation reactions; hydrogenation and reduction of CC bonds; hydrogenation and reduction of zCωO bond; hydrogenation and reduction of CN bond; isomerization and rearrangements; insertion reactions; coupling reaction; (Catecholatoboryl)triethylammonium tetrachloroaluminate; enantioselective halogenation; synthetic chiral ligands; chromium – carbene complexes