
Journal of Organometallic Chemistry p. 273 - 280 (1992)
Update date:2022-08-03
Topics:
Tacke, Reinhold
Wuttke, Frank
Henke, Henning
The stereochemistry of the microbial reduction of rac-acetyl(t-butyl)methylphenylsilane (rac-1) with cells of Trigonopsis variabilis (DSM 70714) and Corynebacterium dioxydans (ATCC 21766) has been studied.The absolute configuration of the diastereomeric biotransformation products (SiR,CR)- and (SiS,CR)-t-butyl(1-hydroxyethyl)methylphenylsilane ((Si,R,CR)-2 and (SiS,CR)-3) has been determined on the basis of a single-crystal X-ray diffraction study of (SiS,CS,C'R)-t-butylmethyl<1-
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