The reaction is typically carried out under specific conditions to ensure stereoselectivity, resulting in the formation of a chiral 1,2,3-aminodial. The stereoselectivity can be controlled through the choice of reagents and reaction conditions.
If you need to purchase chemical raw materials, submit your demand information to get the latest quotations.
(2S,3R,4S)-2-[(tert-butyloxycarbonyl)amino]-1-cyclohexyl-3,4-dihydroxy-6-methylheptane
(1R,5R)-5-isopropenyl-2-methylcyclohex-2-enyl N,N-diisopropylcarbamate
C29H38O6S
(Z)-(4R,5S)-4,5-Dimethyl-7-phenyl-7-trimethylsilanyloxy-hept-6-en-3-one
tert-Butyl-[(2R,3S)-3-(2-methoxy-ethoxymethoxy)-2-methyl-pent-4-enyloxy]-diphenyl-silane
(1R,2R,4aS,5S,8aR)-2-[(5E,7E,9E)-9-(tert-Butyl-diphenyl-silanyloxymethyl)-undeca-5,7,9-trienyl]-5-methoxymethoxy-1-methyl-4-trimethylsilanyl-1,2,4a,5,6,7,8,8a-octahydro-naphthalene-1-carboxylic acid allyl ester
1,3-dimethoxy-2-methyl-5-[(Z)-prop-1-enyl]benzene
(3S,5S,6R)-3-(5-Azido-pentyl)-2-oxo-5,6-diphenyl-morpholine-4-carboxylic acid benzyl ester
[(1R,5S)-5-(2-Bromo-1-ethoxy-ethoxy)-cyclohex-3-enylmethoxymethyl]-benzene
1-Benzenesulfonyl-3-methyl-3-((2R,3R,7S,10R)-2,3,10-trimethyl-1,4,6-trioxa-spiro[4.5]dec-7-yl)-butan-2-one
