An Enzymatic Enantioselective Route to Methyl Carboxylate 2,3 - Methanohomoserine γ-Lactone; A Precursor of Chiral 2,3 - Methanohomoserine
- 1 July 1991
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 21 (14) , 1429-1432
- https://doi.org/10.1080/00397919108016415
Abstract
Enzymatic hydrolysis of Dimethyl 2 - (tetrahydropyranyl) hydroxymethyl cyclopropane 1,1 - dicarboxylate 6 with an industrial esterase, followed by a deprotection of tetrahydropyranyl ether affords the title compound in 20% yield.Keywords
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