Convergent synthesis of the FGHI ring segment of yessotoxin

Isao Kadota, Hirokazu Ueno, Yuki Sato, Yoshinori Yamamoto

Research output: Contribution to journalArticle

20 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 languageEnglish
Pages (from-to)89-92
Number of pages4
JournalTetrahedron Letters
Volume47
Issue number1
DOIs
Publication statusPublished - Jan 2 2006
Externally publishedYes

Fingerprint

Allylation
Ether
yessotoxin

Keywords

  • Convergent synthesis
  • Polycyclic ethers
  • Yessotoxin

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Convergent synthesis of the FGHI ring segment of yessotoxin. / Kadota, Isao; Ueno, Hirokazu; Sato, Yuki; Yamamoto, Yoshinori.

In: Tetrahedron Letters, Vol. 47, No. 1, 02.01.2006, p. 89-92.

Research output: Contribution to journalArticle

Kadota, Isao ; Ueno, Hirokazu ; Sato, Yuki ; Yamamoto, Yoshinori. / Convergent synthesis of the FGHI ring segment of yessotoxin. In: Tetrahedron Letters. 2006 ; Vol. 47, No. 1. pp. 89-92.
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