Convergent synthesis of the FGHI ring segment of yessotoxin

Isao Kadota; Hirokazu Ueno; Yuki Sato; Yoshinori Yamamoto

doi:10.1016/j.tetlet.2005.10.136

Convergent synthesis of the FGHI ring segment of yessotoxin

Isao Kadota, Hirokazu Ueno, Yuki Sato, Yoshinori Yamamoto

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

22 Citations (Scopus)

Abstract

A convergent synthesis of the FGHI ring segment of yessotoxin was achieved via the intramolecular allylation of an α-chloroacetoxy ether and subsequent ring-closing metathesis.

Original language	English
Pages (from-to)	89-92
Number of pages	4
Journal	Tetrahedron Letters
Volume	47
Issue number	1
DOIs	https://doi.org/10.1016/j.tetlet.2005.10.136
Publication status	Published - Jan 2 2006
Externally published	Yes

Keywords

Convergent synthesis
Polycyclic ethers
Yessotoxin

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/j.tetlet.2005.10.136

Cite this

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title = "Convergent synthesis of the FGHI ring segment of yessotoxin",

abstract = "A convergent synthesis of the FGHI ring segment of yessotoxin was achieved via the intramolecular allylation of an α-chloroacetoxy ether and subsequent ring-closing metathesis.",

keywords = "Convergent synthesis, Polycyclic ethers, Yessotoxin",

author = "Isao Kadota and Hirokazu Ueno and Yuki Sato and Yoshinori Yamamoto",

note = "Funding Information: This work was financially supported by a Grant-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology, Japan. ",

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T1 - Convergent synthesis of the FGHI ring segment of yessotoxin

AU - Kadota, Isao

AU - Ueno, Hirokazu

AU - Sato, Yuki

AU - Yamamoto, Yoshinori

N1 - Funding Information: This work was financially supported by a Grant-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology, Japan.

PY - 2006/1/2

Y1 - 2006/1/2

N2 - A convergent synthesis of the FGHI ring segment of yessotoxin was achieved via the intramolecular allylation of an α-chloroacetoxy ether and subsequent ring-closing metathesis.

AB - A convergent synthesis of the FGHI ring segment of yessotoxin was achieved via the intramolecular allylation of an α-chloroacetoxy ether and subsequent ring-closing metathesis.

KW - Convergent synthesis

KW - Polycyclic ethers

KW - Yessotoxin

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M3 - Article

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JO - Tetrahedron Letters

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Convergent synthesis of the FGHI ring segment of yessotoxin

Abstract

Keywords

ASJC Scopus subject areas

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