Isomerization of imines, trifluoromethyl imines, alkyl trifluoromethylated amines, (8α,9R)-2′-Chloro-10,11-dihydro-6′-methoxycinchonan-9-ol, Dihydroquinine DerivativeIsomerization Isomerization of imines, (E)-2,2,2-trifluoro-N-(4-nitrobenzyl)-1-phenylethan-1-imines, (R,E)-1-(4-nitrophenyl)-N-(2,2,2-trifluoro-1-phenylethyl)methanimines, (8α,9R)-2′-Chloro-10,11-dihydro-6′-methoxycinchonan-9-ol, Dihydroquinine DerivativeIsomerization Alkylation, gramine, tert-Butyl N-(diphenylmethylene)glycinate, N-(Diphenylmethylene)-L-tryptophan 1,1-dimethylethyl ester, (8α,9R)-1-(9-anthracenylmethyl)-9- (2-propenyloxy)-Cinchonanium bromide, Cinchonidine DerivativeAlkylation, Alkylation Hydrosilylation, (E)-N,1-diphenylpropan-1-imine, trichlorosilane, (R)-N-(1-phenylpropyl)aniline, 2-[[(8α,9S)-cinchonan-9-ylamino]carbonyl]-1-methyl-Pyridinium tetrafluoroborate, Cinchonidine DerivativeHydrogenation, Hydrogenation of imines, Hydrosilylation Alkylation, methyl 1-oxo-2,3-dihydro-1H-indene-2-carboxylate, ethyl 2,2-difluoro-2-iodoacetate, methyl (R)-2-(2-ethoxy-1,1-difluoro-2-oxoethyl)-1-oxo-2,3-dihydro-1H-indene-2-carboxylate, 1-[2-([1,1′-biphenyl]-2-ylamino)-2-oxoethyl]- 9-hydroxy-(8α,9R)-Cinchonanium bromide, Cinchonidine DerivativeAlkylation, Alkylation Alkylation, tert-butyl (1-benzyl-2-oxoindolin-3-yl)(2-chloroethyl)carbamate, tert-butyl (S)-1′-benzyl-2′-oxospiro[azetidine-2,3′-indoline]-1-carboxylate, (1S,2S,4S,5R)-2-((R)-hydroxy(quinolin-4-yl)methyl)-1-(4-(pentafluoro-l6-sulfaneyl)benzyl)-5-vinylquinuclidin-1-ium bromide, Cinchonidine DerivativeAlkylation, Alkylation, Spirocyclization Arylation, 4-(3-methoxybenzyl)-3-methylisoxazol-5(4H)-one, N,N’-((1E,2Z)-cyclohexa-3,5-diene-1,2-diylidene)dibenzamide, (R)-N,N’-(4-(4-(3-methoxybenzyl)-3-methyl-5-oxo-4,5-dihydroisoxazol-4-yl)-1,2-phenylene)dibenzamide, 3-[[3,5-bis(trifluoromethyl)phenyl]amino]-4-[(8α,9S)-cinchonan-9-ylamino]-3-Cyclobutene-1,2-dione, Cinchonidine DerivativeArylation, Further reactions Vinylogous Michael Addition, tert-butyl 2-oxo-3-(propan-2-ylidene)indoline-1-carboxylate, 5-(chloromethyl)-3-methyl-4-nitroisoxazole, tert-butyl (1R,3S)-2,2-dimethyl-3-(3-methyl-4-nitroisoxazol-5-yl)-2′-oxospiro[cyclopropane-1,3′-indoline]-1′-carboxylate, N-[3,5-Bis(trifluoromethyl)phenyl]-N′-(8α,9S)-cinchonan-9-ylurea, Cinchonidine DerivativeCyclopropanation, Michael Addition, Vinylogous Michael Addition Racemic resolution, 4-cyano-4-(4-nitrophenyl)hexanoic acid, (R)-4-cyano-4-(4-nitrophenyl)hexanoic acid, Cinchonidine BaseRacemic resolution, Resolution Michael Addition, tert-butyl 3-fluoro-2-oxoindoline-1-carboxylates, 4-benzylidene-2,6-di-tert-butylcyclohexa-2,5-dien-1-ones, tert-butyl (R)-3-((S)-(3,5-di-tert-butyl-4-hydroxyphenyl)(phenyl)methyl)-3-fluoro-2-oxoindoline-1-carboxylates, O-Allyl-1-(anthracen-9-ylmethyl)-cinchonidinium bromide, Cinchonidine DerivativeMichael, Michael Addition« Older EntriesNext Entries »
Isomerization of imines, trifluoromethyl imines, alkyl trifluoromethylated amines, (8α,9R)-2′-Chloro-10,11-dihydro-6′-methoxycinchonan-9-ol, Dihydroquinine DerivativeIsomerization
Isomerization of imines, (E)-2,2,2-trifluoro-N-(4-nitrobenzyl)-1-phenylethan-1-imines, (R,E)-1-(4-nitrophenyl)-N-(2,2,2-trifluoro-1-phenylethyl)methanimines, (8α,9R)-2′-Chloro-10,11-dihydro-6′-methoxycinchonan-9-ol, Dihydroquinine DerivativeIsomerization
Alkylation, gramine, tert-Butyl N-(diphenylmethylene)glycinate, N-(Diphenylmethylene)-L-tryptophan 1,1-dimethylethyl ester, (8α,9R)-1-(9-anthracenylmethyl)-9- (2-propenyloxy)-Cinchonanium bromide, Cinchonidine DerivativeAlkylation, Alkylation
Hydrosilylation, (E)-N,1-diphenylpropan-1-imine, trichlorosilane, (R)-N-(1-phenylpropyl)aniline, 2-[[(8α,9S)-cinchonan-9-ylamino]carbonyl]-1-methyl-Pyridinium tetrafluoroborate, Cinchonidine DerivativeHydrogenation, Hydrogenation of imines, Hydrosilylation
Alkylation, methyl 1-oxo-2,3-dihydro-1H-indene-2-carboxylate, ethyl 2,2-difluoro-2-iodoacetate, methyl (R)-2-(2-ethoxy-1,1-difluoro-2-oxoethyl)-1-oxo-2,3-dihydro-1H-indene-2-carboxylate, 1-[2-([1,1′-biphenyl]-2-ylamino)-2-oxoethyl]- 9-hydroxy-(8α,9R)-Cinchonanium bromide, Cinchonidine DerivativeAlkylation, Alkylation
Alkylation, tert-butyl (1-benzyl-2-oxoindolin-3-yl)(2-chloroethyl)carbamate, tert-butyl (S)-1′-benzyl-2′-oxospiro[azetidine-2,3′-indoline]-1-carboxylate, (1S,2S,4S,5R)-2-((R)-hydroxy(quinolin-4-yl)methyl)-1-(4-(pentafluoro-l6-sulfaneyl)benzyl)-5-vinylquinuclidin-1-ium bromide, Cinchonidine DerivativeAlkylation, Alkylation, Spirocyclization
Arylation, 4-(3-methoxybenzyl)-3-methylisoxazol-5(4H)-one, N,N’-((1E,2Z)-cyclohexa-3,5-diene-1,2-diylidene)dibenzamide, (R)-N,N’-(4-(4-(3-methoxybenzyl)-3-methyl-5-oxo-4,5-dihydroisoxazol-4-yl)-1,2-phenylene)dibenzamide, 3-[[3,5-bis(trifluoromethyl)phenyl]amino]-4-[(8α,9S)-cinchonan-9-ylamino]-3-Cyclobutene-1,2-dione, Cinchonidine DerivativeArylation, Further reactions
Vinylogous Michael Addition, tert-butyl 2-oxo-3-(propan-2-ylidene)indoline-1-carboxylate, 5-(chloromethyl)-3-methyl-4-nitroisoxazole, tert-butyl (1R,3S)-2,2-dimethyl-3-(3-methyl-4-nitroisoxazol-5-yl)-2′-oxospiro[cyclopropane-1,3′-indoline]-1′-carboxylate, N-[3,5-Bis(trifluoromethyl)phenyl]-N′-(8α,9S)-cinchonan-9-ylurea, Cinchonidine DerivativeCyclopropanation, Michael Addition, Vinylogous Michael Addition
Racemic resolution, 4-cyano-4-(4-nitrophenyl)hexanoic acid, (R)-4-cyano-4-(4-nitrophenyl)hexanoic acid, Cinchonidine BaseRacemic resolution, Resolution
Michael Addition, tert-butyl 3-fluoro-2-oxoindoline-1-carboxylates, 4-benzylidene-2,6-di-tert-butylcyclohexa-2,5-dien-1-ones, tert-butyl (R)-3-((S)-(3,5-di-tert-butyl-4-hydroxyphenyl)(phenyl)methyl)-3-fluoro-2-oxoindoline-1-carboxylates, O-Allyl-1-(anthracen-9-ylmethyl)-cinchonidinium bromide, Cinchonidine DerivativeMichael, Michael Addition
