Sec-alkyl sulfate esters

Among the latter group. Pseudomonas sp. DSM 6611 was identified as top candidate by displaying excellent stereo- and enantio-selectivities for a range of sec-alkyl sulfate esters by transforming the (7 )-enantiomer of the rac-sulfate ester into the corresponding (5)-alcohol (Scheme 3.2). ... [Pg.117]

S.R., and Faber, K. (2002) Enantiose-lective stereoinversion in the kinetic resolution of rac-sec-alkyl sulfate esters by hydrolysis with an alkyl-sulfatase from rhodococcus ruber DSM 44541 furnishes homochiral products. Angew. Chem. Int. Ed., 41 (21), 4052-4054. [Pg.160]

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