An enantioselective total synthesis of aspergillides A and B

Haruhiko Fuwa; Hiroshi Yamaguchi; Makoto Sasaki

doi:10.1016/j.tet.2010.07.062

An enantioselective total synthesis of aspergillides A and B

Haruhiko Fuwa, Hiroshi Yamaguchi, Makoto Sasaki

Research output: Contribution to journal › Article › peer-review

43 Citations (Scopus)

Abstract

An enantioselective total synthesis of aspergillides A and B has been accomplished on the basis of a unified synthetic strategy that exploits stereodivergent intramolecular oxa-conjugate cyclization and Yamaguchi macrolactonization.

Original language	English
Pages (from-to)	7492-7503
Number of pages	12
Journal	Tetrahedron
Volume	66
Issue number	38
DOIs	https://doi.org/10.1016/j.tet.2010.07.062
Publication status	Published - 2010 Sep 18

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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abstract = "An enantioselective total synthesis of aspergillides A and B has been accomplished on the basis of a unified synthetic strategy that exploits stereodivergent intramolecular oxa-conjugate cyclization and Yamaguchi macrolactonization.",

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AU - Yamaguchi, Hiroshi

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