- Highly diastereo- and enantio-selective epoxidation of secondary allylic alcohols catalyzed by styrene monooxygenase.
Highly diastereo- and enantio-selective epoxidation of secondary allylic alcohols catalyzed by styrene monooxygenase.
Chemical communications (Cambridge, England) (2011-01-15)
Hui Lin, Yan Liu, Zhong-Liu Wu
PMID21234475
ABSTRACT
Enantiomerically enriched glycidol derivatives with contiguous stereogenic centers were obtained in a highly diastereo- and enantio-selective epoxidation catalyzed with the styrene monooxygenase StyAB2.
MATERIALS