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An asymmetric synthesis of all stereoisomers of piclavines A1-4 using an iterative asymmetric dihydroxylation.

ABSTRACT: The asymmetric synthesis of both enantiomers of piclavines A1, A2, A3, and A4 has been achieved using an iterative asymmetric dihydroxylation with enantiomeric enhancement.

SUBMITTER: Saito Y

PROVIDER: S-EPMC2200665 | biostudies-literature | 2007 Oct

REPOSITORIES: biostudies-literature

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An asymmetric synthesis of all stereoisomers of piclavines A1-4 using an iterative asymmetric dihydroxylation.

Saito Yukako Y Okamoto Naoki N Takahata Hiroki H

Beilstein journal of organic chemistry 20071029

The asymmetric synthesis of both enantiomers of piclavines A1, A2, A3, and A4 has been achieved using an iterative asymmetric dihydroxylation with enantiomeric enhancement. ...[more]

PMID: 17967195

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