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

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

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

Bibliographic Details
Main Authors:	Yukako Saito, Naoki Okamoto, Hiroki Takahata
Format:	Article
Language:	English
Published:	Beilstein-Institut 2007-10-01
Series:	Beilstein Journal of Organic Chemistry
Online Access:	https://doi.org/10.1186/1860-5397-3-37

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