In:
ChemCatChem, Wiley, Vol. 3, No. 2 ( 2011-02-07), p. 343-346
Abstract:
Both enantiomers of various 1‐aryl‐1,2‐ethanediols have been prepared in a one‐pot method from the corresponding arylethanones through the combination of chemical and enzymatic reactions. A range of aryl groups, phenyl, 4‐chlorophenyl, benzo[ b ]thiophene‐3‐yl, and benzofuran‐2‐yl, were used. The highly enantiomerically enriched ( R )‐ and ( S )‐1‐aryl‐1,2‐ethanediols were obtained with excellent yields, calculated for the arylethanones.
Type of Medium:
Online Resource
ISSN:
1867-3880
,
1867-3899
DOI:
10.1002/cctc.201000295
Language:
English
Publisher:
Wiley
Publication Date:
2011
detail.hit.zdb_id:
2501161-3
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