Convergent synthesis of the A-F ring segment of yessotoxin and adriatoxin

Isao Kadota, Hirokazu Ueno, Yoshinori Yamamoto

Research output: Contribution to journalArticle

29 Citations (Scopus)

Abstract

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

Original languageEnglish
Pages (from-to)8935-8938
Number of pages4
JournalTetrahedron Letters
Volume44
Issue number50
DOIs
Publication statusPublished - Dec 8 2003
Externally publishedYes

Fingerprint

Allylation
Ether
adriatoxin
yessotoxin

Keywords

  • Adriatoxin
  • Convergent synthesis
  • Polycyclic ethers
  • Yessotoxin

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Convergent synthesis of the A-F ring segment of yessotoxin and adriatoxin. / Kadota, Isao; Ueno, Hirokazu; Yamamoto, Yoshinori.

In: Tetrahedron Letters, Vol. 44, No. 50, 08.12.2003, p. 8935-8938.

Research output: Contribution to journalArticle

Kadota, Isao ; Ueno, Hirokazu ; Yamamoto, Yoshinori. / Convergent synthesis of the A-F ring segment of yessotoxin and adriatoxin. In: Tetrahedron Letters. 2003 ; Vol. 44, No. 50. pp. 8935-8938.
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