Enantioselective synthesis of cyclic amino alcohols

Organic compounds -- part of the class 532-570 series – Organic compounds – Amino nitrogen containing

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564415, 564428, C07C20940

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055741860

ABSTRACT:
There is disclosed a novel process for the enantioselective synthesis of chiral amino alcohols from keto oxime ethers, which are derived from cyclic ketones, via catalytic asymmetric reduction, employing oxazaborolidine-borane complex (OAB-BH.sub.3). In this catalytic reduction process two chiral centers are created in a single step with high levels of stereoselectivity.

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