![Sample our Physical Sciences journals, sign in here to start your FREE access for 14 days]({"type":"image" , "src" : "/sda/110819/TOC-Subject-Sample-2021-Physical-Sciences.jpg"})
Abstract
Regioselective reduction of racemic epoxides to optically active alcohols using chirally modified zirconium tetrachloride - sodium borohydride with L-proline.
Notes
IICT Communication No. 3632
Asymmetric reduction of oxime ethers with chirally modified zirconium tetrachloride - sodium borohydride using α-amino alcohols is the only example reported earlier1.