This term implies that the molecules involved in the reaction have the same chirality or handedness. In the context of organic chemistry, chirality is often associated with stereoisomers, particularly enantiomers.
If you need to purchase chemical raw materials, submit your demand information to get the latest quotations.
(5S,6R)-5-((Z)-2-Benzyloxymethoxy-vinyl)-dodecan-6-ol
1,2-Butanediol, 3-methyl-, (2S)-
(3R,αS,E)-tert-butyl 3-(N-benzyl-N-α-methylbenzylamino)-3-[4-(3-tert-butoxy-3-oxoprop-1-enyl)phenyl]propanoate
(2S,3R)-3-fluoro-1-<(4-methylphenyl)sulfenyl>-5-hexen-2-ol
[(S)-3-(tert-Butyl-dimethyl-silanyloxy)-1-(4-methoxy-benzoyl)-propyl]-carbamic acid benzyl ester
(2S,3S)-3-METHYLPYRROLIDINE-2-CARBOXYLIC ACID
1-Cyclopentene-1-carboxylic acid, 3-(phenylmethyl)-, 1,1-dimethylethyl ester
(2R,4S)-2-tert-Butyl-3-phenylacetyl-4-methoxycarbonyl-1,3-oxazolidine
<<(+)-menthyloxy>(tosyloxy)iodo>benzene
(S,S)-1,3-propanediylbis<(o-methoxyphenyl)phenylphosphine>
(2S,4R)-3-benzoyl-4-butyl-2-phenyloxazolidin-5-one
2-cyclopenten-1-one (S,S)-1,2-diphenyl-1,2-ethanediol ketal
(S)-tert-butyl 2-((tert-butyldiphenylsilyloxy)Methyl)-5-oxo-2,5-dihydro-1H-pyrrole-1-carboxylate
Butanoic acid, 3-[[(1R)-1-phenylethyl](phenylmethyl)amino]-, 1,1-dimethylethyl ester, (3R)-
(3S)-3-fluoro-6-methyl-1-<(R)-(4-methylphenyl)sulphinyl>-2-heptanone
(4R,5R)-4,5-bis(iodomethyl)cyclohexene
(2S,4S)-2,4-bis(tert-butoxycarbonyl)-1-(4-bromobenzoyl)pyrrolidine
