Epoxidation, 2-isopropylnaphthalene-1,4-dione, hydrogen peroxide, (1aS,7aR)-1a-isopropyl-1a,7a-dihydronaphtho[2,3-b]oxirene-2,7-dione, (9S)-1-(9-anthracenylmethyl)-9-hydroxy-cinchonanium chloride, Cinchonine DerivativeEpoxidation Aldol reaction, 1-naphthalenecarboxaldehyde, tert-butyl diazoacetate, 1,1-dimethylethyl (βS)-α-diazo-β-hydroxybenzenepropanoate, (8α,9R)- 1-(9-anthracenylmethyl)- 9-hydroxy-Cinchonanium chloride, Cinchonidine DerivativeAldol, Aldol Alkylation, o-biphenyl-2-oxazoline-4-carboxylic acid tert-butyl ester, 3-bromoprop-1-ene, (bromomethyl)benzene, substituited o-biphenyl-2-oxazoline-4-carboxylic acid tert-butyl ester, 1-(9-anthracenylmethyl)-9-(2-propenyloxy)-(8α,9R)-cinchonanium bromide, Dihydrocinchonidine DerivativeAlkylation, Alkylation Aziridination, 1-((4R,7S)-7-isopropyl-4-methyl-3-phenyl-4,5,6,7-tetrahydro-1H-indazol-1-yl)prop-2-en-1-one, N-chloro-N-sodiocarbamates, benzyl (S)-2-((4R,7S)-7-isopropyl-4-methyl-3-phenyl-4,5,6,7-tetrahydro-1H-indazole-1-carbonyl)aziridine-1-carboxylate, 1-(9-anthracenylmethyl)-9-(2-propenyloxy)-(8α,9R)-cinchonanium bromide, Cinchonidine DerivativeAziridination Spirocyclization, substituted cyclopent-2-en-1-one, substituted isoxazol-5(4H)-one, aldehydes, substituted tetrahydro-4’H,5H-spiro[isoxazole-4,2′-pentalene]-4′,5-dione, 4-methylsalicylic acid, (8α,9S)-2′-(1,1-Dimethylethyl)cinchonan-9-amine, Cinchonidine DerivativeSpirocyclization Oxysulfonation, substituted (Z)-but-3-enal oxime, sulfonylchlorides, substituted sulfonylmethyl-4,5-dihydroisoxazole, N-(8α,9S)-Cinchonan-9-yl-2,3,5,6-tetramethylbenzenesulfonamide, Cinchonidine DerivativeCyclization, Further reactions, Isoxazoline cyclization, Oxysulfonylation Iodination, substituted (1Z,3E)-hexa-3,5-dienal oxime, N-Iodsuccinimid, substituted (R,E)-5-(3-iodoprop-1-en-1-yl)-4,5-dihydroisoxazole, N-[3,5-bis(trifluoromethyl)phenyl]-N′-[(8α,9S)-10,11- dihydro-11-phenylcinchonan-9-yl]-thiourea, Cinchonidine DerivativeCyclization, Iodination, Iodoetherification, Isoxazoline cyclization Chlorocyclization, substituted o-vinylanilide, 1,3-dichloro-5,5-dimethylimidazolidine-2,4-dione, substituted chloromethyl-2-phenyl-4H-benzoxazine, 9-[2-[bis(2-methylphenyl)amino]benzoate]-(8α,9R)-cinchonan-9-ol, Cinchonidine DerivativeChlorination, Cyclization α-Hydroxylation, β‐dicarbonyl compounds, 2-hydroxy-1-oxo-2,3-dihydro-1H-indene-2-carboxylic acid ester, tetraphenylporphyrin, 1-[(3,5-dibromophenyl)methyl]-9-hydroxy-2′-(2-naphthalenyl)-(9S)-cinchonanium bromide, Cinchonine DerivativeHydroxylation Assymetric Arylation, substituted 2-oxocyclopentane-1-carboxylic acid ester, substituted 1-fluoro-2-nitrobenzene, substituted 1-(2-nitrophenyl)-2-oxocyclopentane-1-carboxylic acid ester, 9-(benzoyloxy)-1-(phenylmethyl)-(8α,9R)-cinchonanium bromide, Cinchonidine DerivativeArylation, Further reactions« Older EntriesNext Entries »
Epoxidation, 2-isopropylnaphthalene-1,4-dione, hydrogen peroxide, (1aS,7aR)-1a-isopropyl-1a,7a-dihydronaphtho[2,3-b]oxirene-2,7-dione, (9S)-1-(9-anthracenylmethyl)-9-hydroxy-cinchonanium chloride, Cinchonine DerivativeEpoxidation
Aldol reaction, 1-naphthalenecarboxaldehyde, tert-butyl diazoacetate, 1,1-dimethylethyl (βS)-α-diazo-β-hydroxybenzenepropanoate, (8α,9R)- 1-(9-anthracenylmethyl)- 9-hydroxy-Cinchonanium chloride, Cinchonidine DerivativeAldol, Aldol
Alkylation, o-biphenyl-2-oxazoline-4-carboxylic acid tert-butyl ester, 3-bromoprop-1-ene, (bromomethyl)benzene, substituited o-biphenyl-2-oxazoline-4-carboxylic acid tert-butyl ester, 1-(9-anthracenylmethyl)-9-(2-propenyloxy)-(8α,9R)-cinchonanium bromide, Dihydrocinchonidine DerivativeAlkylation, Alkylation
Aziridination, 1-((4R,7S)-7-isopropyl-4-methyl-3-phenyl-4,5,6,7-tetrahydro-1H-indazol-1-yl)prop-2-en-1-one, N-chloro-N-sodiocarbamates, benzyl (S)-2-((4R,7S)-7-isopropyl-4-methyl-3-phenyl-4,5,6,7-tetrahydro-1H-indazole-1-carbonyl)aziridine-1-carboxylate, 1-(9-anthracenylmethyl)-9-(2-propenyloxy)-(8α,9R)-cinchonanium bromide, Cinchonidine DerivativeAziridination
Spirocyclization, substituted cyclopent-2-en-1-one, substituted isoxazol-5(4H)-one, aldehydes, substituted tetrahydro-4’H,5H-spiro[isoxazole-4,2′-pentalene]-4′,5-dione, 4-methylsalicylic acid, (8α,9S)-2′-(1,1-Dimethylethyl)cinchonan-9-amine, Cinchonidine DerivativeSpirocyclization
Oxysulfonation, substituted (Z)-but-3-enal oxime, sulfonylchlorides, substituted sulfonylmethyl-4,5-dihydroisoxazole, N-(8α,9S)-Cinchonan-9-yl-2,3,5,6-tetramethylbenzenesulfonamide, Cinchonidine DerivativeCyclization, Further reactions, Isoxazoline cyclization, Oxysulfonylation
Iodination, substituted (1Z,3E)-hexa-3,5-dienal oxime, N-Iodsuccinimid, substituted (R,E)-5-(3-iodoprop-1-en-1-yl)-4,5-dihydroisoxazole, N-[3,5-bis(trifluoromethyl)phenyl]-N′-[(8α,9S)-10,11- dihydro-11-phenylcinchonan-9-yl]-thiourea, Cinchonidine DerivativeCyclization, Iodination, Iodoetherification, Isoxazoline cyclization
Chlorocyclization, substituted o-vinylanilide, 1,3-dichloro-5,5-dimethylimidazolidine-2,4-dione, substituted chloromethyl-2-phenyl-4H-benzoxazine, 9-[2-[bis(2-methylphenyl)amino]benzoate]-(8α,9R)-cinchonan-9-ol, Cinchonidine DerivativeChlorination, Cyclization
α-Hydroxylation, β‐dicarbonyl compounds, 2-hydroxy-1-oxo-2,3-dihydro-1H-indene-2-carboxylic acid ester, tetraphenylporphyrin, 1-[(3,5-dibromophenyl)methyl]-9-hydroxy-2′-(2-naphthalenyl)-(9S)-cinchonanium bromide, Cinchonine DerivativeHydroxylation
Assymetric Arylation, substituted 2-oxocyclopentane-1-carboxylic acid ester, substituted 1-fluoro-2-nitrobenzene, substituted 1-(2-nitrophenyl)-2-oxocyclopentane-1-carboxylic acid ester, 9-(benzoyloxy)-1-(phenylmethyl)-(8α,9R)-cinchonanium bromide, Cinchonidine DerivativeArylation, Further reactions
