a chemical process that uses a catalyst to create a chiral molecule with a specific stereochemistry.
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(2R,4R,6R,8R)-2,4,6,8-Tetramethyl-1-octacosanol
benzyl 4-bromo-3,5-bis(benzyloxy)benzoate
L-Alanine, N-[N-(trifluoroacetyl)-D-phenylalanyl]-, methyl ester
(R)-(+)-2-(N-Benzyl-N-benzyloxycarbamoylmethyl)heptanoic acid
(R)-1-(methoxymethyl)-3-(2-(naphthalen-1-yl)-2-oxo-1-phenylethyl)quinolin-2(1H)-one
Cyclohexanone, 2-(2,3,4-trimethoxyphenyl)-
(R)-4-((2R,3S)-3-((benzyloxy)methyl)oxiran-2-yl)-2,2-dimethyl-1,3-dioxolane
1,2-Butanediamine,N1,N1,3-trimethyl-,(2R)-(9CI)
C19H25NO5S
trans-(3R,4S)-1(R)-(α-methylbenzyl)-3-(2,2,5,5-tetramethyl-1-aza-2,5-disilacyclopentyl)-4-(2-pyridyl)-2-azetidinone
((1S,2R,3S,4R)-1-Benzyl-4-tert-butoxycarbonylamino-2,3-dihydroxy-5-phenyl-pentyl)-carbamic acid tert-butyl ester
Benzoic acid, 3,5-bis[[(1,1-dimethylethyl)dimethylsilyl]oxy]-4-methoxy-, methyl ester
ethyl (Z)-2-phenyl-3-(trifluoromethylsulfonyloxy)but-2-enoate
(S,S)-2,4-bis<(tert-butyldimethylsiloxy)methyl>-N-<(S)-1-phenylethyl>azetidine
3-[(TriMethylsilyl)ethynyl]aniline
FEMA 2763
