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ChemInform Abstract: Synthetic Studies of the Lichen Macrolide Lepranthin. Stereoselective Synthesis of the Diolide Framework Based on Regioselective Epoxide-Opening Reactions.

✍ Scribed by Hisashi Takada; Shinji Nagumo; Eiko Yasui; Megumi Mizukami; Masaaki Miyashita

Publisher: John Wiley and Sons
Year: 2011
Weight: 40 KB
Volume: 42
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.201141188

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✦ Synopsis

Abstract

A synthetic approach toward 16‐membered diolide (VIIb), a fully functionalized congener of Lepranthin (VIIa), is developed.

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