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

Yukako Saito; Naoki Okamoto; Hiroki Takahata

doi:10.1186/1860-5397-3-37

Beilstein Journal of Organic Chemistry (Oct 2007)

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

Yukako Saito,
Naoki Okamoto,
Hiroki Takahata

Affiliations

Yukako Saito: Faculty of Pharmaceutical Sciences, Tohoku Pharmaceutical University, Sendai 981-8558, Japan
Naoki Okamoto: Faculty of Pharmaceutical Sciences, Tohoku Pharmaceutical University, Sendai 981-8558, Japan
Hiroki Takahata: Faculty of Pharmaceutical Sciences, Tohoku Pharmaceutical University, Sendai 981-8558, Japan

DOI: https://doi.org/10.1186/1860-5397-3-37
Journal volume & issue: Vol. 3, no. 1
p. 37

Abstract

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

Published in Beilstein Journal of Organic Chemistry

ISSN: 1860-5397 (Online)
Publisher: Beilstein-Institut
Country of publisher: Germany
LCC subjects: Science: Chemistry: Organic chemistry
Website: http://www.beilstein-journals.org/bjoc

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