Stereoselectivity in a reaction means that it favors the formation of a particular stereoisomer (a molecule with the same atoms but arranged differently in space). "Highly stereoselective" indicates that the reaction is particularly good at producing a specific stereoisomer with minimal formation of other stereoisomers.
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1-(4-chloro-butylidene)-2-(toluene-4-sulfonyl)-2,3,4,9-tetrahydro-1H-β-carboline
1,2-diphenyl-2-phenylsulfinyl ethanol
(4S,5R,6S)-2,4-Dimethyl-5-hydroxy-6-(p-methoxyphenyl)-1-hepten-3-one
3-(1H-indol-3-yl)-2-methyl-3-phenylpropan-1-ol
(2R,3S,4S,5S,6S)-3,4,5-Tris-benzyloxy-2-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-6-methoxy-tetrahydro-pyran
1-Pyrrolidinecarboxylic acid, 2-[(1R)-1-hydroxy-2-(2S)-oxiranylethyl]-, phenylmethyl ester, (2S)-
