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Published in 2017 at "Catalysts"
DOI: 10.3390/catal7020037
Abstract: A two-step stereoselective chemoenzymatic synthesis of optically active α-aryl-substituted oxygen heterocycles was developed, exploiting a whole-cell mediated asymmetric reduction of α-, β-, and γ-chloroalkyl arylketones followed by a stereospecific cyclization of the corresponding chlorohydrins into…
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Keywords:
optically active;
oxygen;
synthesis optically;
aryl substituted ... See more keywords