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 › peer-review

16 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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title = "Stereoselective synthesis of zoanthenol ABC-ring by radical strategy",

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",

note = "Funding Information: This work was supported financially by a Grant-in-Aid for Scientific Research (B) and (C) from the Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan, and the Suntory Foundation for Life Sciences. ",

year = "2013",

month = mar,

day = "13",

doi = "10.1016/j.tetlet.2012.12.104",

language = "English",

volume = "54",

pages = "1389--1391",

journal = "Tetrahedron Letters",

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TY - JOUR

T1 - Stereoselective synthesis of zoanthenol ABC-ring by radical strategy

AU - Yamashita, Shuji

AU - Suda, Naoki

AU - Hayashi, Yujiro

AU - Hirama, Masahiro

N1 - Funding Information: This work was supported financially by a Grant-in-Aid for Scientific Research (B) and (C) from the Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan, and the Suntory Foundation for Life Sciences.

PY - 2013/3/13

Y1 - 2013/3/13

N2 - 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.

AB - 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.

KW - Atom transfer

KW - Marine natural product

KW - Tandem radical cyclization

KW - Zoanthenol

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U2 - 10.1016/j.tetlet.2012.12.104

DO - 10.1016/j.tetlet.2012.12.104

M3 - Article

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VL - 54

SP - 1389

EP - 1391

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 11

ER -

Stereoselective synthesis of zoanthenol ABC-ring by radical strategy

Abstract

Keywords

ASJC Scopus subject areas

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