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Atropisomer Synthesis, naphthamides, substituted 2-(((tert-butoxycarbonyl)oxy)methyl)acrylate, axially chiral naphthamides, Dihydroquinine Base

Alkylation, Allylic Alkylation, Atropisomer synthesis

1,4-Hydrophosphinylation, H-phosphine oxides, substituted 2-(tosylmethyl)aniline, substituted (2-aminobenzyl)phosphine oxide, Dihydroquinine Base

Further reactions, Hydrophosphinylation, Phosphination

Michael Addition, β‐oxo phosphonate, nitro olefins, substituted (R)-(4-nitro-1-oxo-1-phenylbutan-2-yl)phosphonate, N-[3,5-Bis(trifluoromethyl)phenyl]-N′-(8α,9S)-cinchonan-9-ylthiourea, Cinchonidine Derivative

Michael, Michael Addition

Sulfa-Michael Addition, α-substituted N-acryloyloxazolidinones, thioacetic acid, S-(3-oxo-3-(2-oxooxazolidin-3-yl)propyl) ethanethioate, N-[3,5-Bis(trifluoromethyl)phenyl]-N′-(8α,9S)-cinchonan-9-ylthiourea, Cinchonidine Derivative

Michael Addition, Sulfa-Michael, Sulfa-Michael Addition

Michael Addition, methyl 2-oxocyclopentane-1-carboxylate, (E)-(2-nitrovinyl)benzene, methyl (S)-1-((R)-2-nitro-1-phenylethyl)-2-oxocyclopentane-1-carboxylate, N-((S)-quinolin-4-yl((1S,2S,4S,5R)-5-vinylquinuclidin-2-yl)methyl)-1-(3-((N-((1S)-quinolin-4-yl((5R)-5-vinylquinuclidin-2-yl)methyl)sulfamoyl)methyl)phenyl)methanesulfonamide, Cinchonidine Derivative

Michael, Michael Addition

Alkylation, substituted 3-((diphenylmethylene)amino)indolin-2-one, substituted 4-benzylidene-2,6-di-tert-butylcyclohexa-2,5-dien-1-one, substituted (R)-3-((R)-(3,5-di-tert-butyl-4-hydroxyphenyl)(phenyl)methyl)-3-((diphenylmethylene)amino)indolin-2-one, (8α,9R)-1-(9-anthracenylmethyl)-9-(2-propenyloxy)-Cinchonanium bromide, Cinchonidine Derivative

Alkylation, alpha-Alkylation

Aza-Diels-Alder, (E)-(buta-1,3-dien-1-yloxy)trimethylsilanes, substituted (Z)-4-methyl-N-(2-methylenebenzofuran-3(2H)-ylidene)benzenesulfonamide, substituted (2R,3S)-1-tosyl-3-vinyl-1,2,3,4-tetrahydrobenzofuro[3,2-b]pyridin-2-ol, 3-[[3,5-bis(trifluoromethyl)phenyl]amino]-4-[(8α,9S)-cinchonan-9-ylamino]-3-Cyclobutene-1,2-dione, Cinchonidine Derivative

Cycloaddition, Diels-Alder reaction

Alkylation, glycine imines, benzyl bromide, tert-butyl (S)-2-((diphenylmethylene)amino)-3-phenylpropanoate, (9S)-(9′′S)-1,1′′-[oxybis(4,1-phenylenemethylene)]bis[9-(2-propen-1-yloxy)-cinchonanium bromide, Cinchonidine Derivative

Alkylation, alpha-Alkylation

Alkylation, 3-amino oxindole, benzyl bromide, (R)-3-benzyl-3-((diphenylmethylene)amino)-1-phenylindolin-2-one, (8α,9R)-(8′′α,9′′R)-1,1′′-[(2-fluoro-1,3-phenylene)bis(methylene)]bis[9-(2-propenyloxy)-cinchonanium dibromide, Cinchonidine Derivative

Alkylation, alpha-Alkylation

Reduction, 1-(4-ethylphenyl)ethan-1-one, (S)-1-(4-ethylphenyl)ethan-1-ol, manganese catalyst, (R)-N-(furan-2-ylmethyl)-1-(quinolin-4-yl)-1-((1S,2R,4S,5R)-5-vinylquinuclidin-2-yl)methanamine, Cinchonine Derivative

Hydrogenation, Hydrogenation of ketones

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