Volume 31, Issue 12
Natural Products
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ChemInform Abstract: A New Diastereoselective Synthesis of a 1β-Methylcarbapenem Intermediate.

Chang-Young Oh

Chang-Young Oh

Coll. Pharm., Sung Kyun Kwan Univ., Suwon 440-746, S. Korea

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Won-Hun Ham

Won-Hun Ham

Coll. Pharm., Sung Kyun Kwan Univ., Suwon 440-746, S. Korea

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First published: 09 June 2010

Abstract

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ChemInform Abstract

A new method for the synthesis of 1β-methylcarbapenem key intermediate (XII) starting from commercially available methyl (R)-3-hydroxybutyrate (I) is given. The key features in this strategy are the diastereoselective alkylation of the dianion of the β-hydroxy ester (I), Sharpless asymmetric epoxidation, and subsequent regioselective cuprate ring opening of the chiral epoxide (VIII) formed.

chemical structure image

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