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Synthesis of mevalonolactone (hiochic acid lactone) employing asymmetric epoxidation as the key-step
Authors:Kenji Mori  Katsuhide Okada
Affiliation:Department of Agricultural Chemistry, The University of Tokyo, Yayoi 1-1-1, Bunkyo-ku, Tokyo 113 Japan
Abstract:(R)( — )-Mevalonolactone (hiochic acid lactone)of 91–93%e.e. was synthesized from an achiral starting material employing the Sharpless asymmetric epoxidation as the key-step.
Keywords:Present address : Laboratory of Food Science   Faculty of Education   amagata University   Yamagata 990   Japan.
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