Stereoselective synthesis of zoanthenol ABC-ring by radical strategy

Shuji Yamashita; Naoki Suda; Yujiro Hayashi; Masahiro Hirama

doi:10.1016/j.tetlet.2012.12.104

Stereoselective synthesis of zoanthenol ABC-ring by radical strategy

Shuji Yamashita, Naoki Suda, Yujiro Hayashi, Masahiro Hirama

SCI - Chemistry

Research output: Contribution to journal › Article

12 Citations (Scopus)

Abstract

Zoanthenol, isolated from Zoanthus sp., possesses an extremely complex architecture including congested quaternary carbons. We describe a concise synthesis of the fully functionalized ABC-ring of zoanthenol based on sequential radical reactions.

Original language	English
Pages (from-to)	1389-1391
Number of pages	3
Journal	Tetrahedron Letters
Volume	54
Issue number	11
DOIs	https://doi.org/10.1016/j.tetlet.2012.12.104
Publication status	Published - 2013 Mar 13

Keywords

Atom transfer
Marine natural product
Tandem radical cyclization
Zoanthenol

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/j.tetlet.2012.12.104

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Yamashita, S., Suda, N., Hayashi, Y., & Hirama, M. (2013). Stereoselective synthesis of zoanthenol ABC-ring by radical strategy. Tetrahedron Letters, 54(11), 1389-1391. https://doi.org/10.1016/j.tetlet.2012.12.104

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abstract = "Zoanthenol, isolated from Zoanthus sp., possesses an extremely complex architecture including congested quaternary carbons. We describe a concise synthesis of the fully functionalized ABC-ring of zoanthenol based on sequential radical reactions.",

keywords = "Atom transfer, Marine natural product, Tandem radical cyclization, Zoanthenol",

author = "Shuji Yamashita and Naoki Suda and Yujiro Hayashi and Masahiro Hirama",

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AU - Yamashita, Shuji

AU - Suda, Naoki

AU - Hayashi, Yujiro

AU - Hirama, Masahiro

PY - 2013/3/13

Y1 - 2013/3/13

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KW - Marine natural product

KW - Tandem radical cyclization

KW - Zoanthenol

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