Convergent synthesis of the ABC-ring moiety of zoanthenol: Intramolecular Mizoroki-Heck reaction

Go Hirai, Hiroki Oguri, Sameh M. Moharram, Koji Koyama, Masahiro Hirama

Research output: Contribution to journalArticle

17 Citations (Scopus)

Abstract

The highly congested ABC-ring moiety of zoanthenol was stereoselectively synthesized via an alkoxylithium-mediated coupling between the A-ring and C-ring moieties followed by a Mizoroki-Heck-type ring closure.

Original languageEnglish
Pages (from-to)5783-5787
Number of pages5
JournalTetrahedron Letters
Volume42
Issue number33
DOIs
Publication statusPublished - Aug 13 2001
Externally publishedYes

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zoanthenol

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

Cite this

Convergent synthesis of the ABC-ring moiety of zoanthenol : Intramolecular Mizoroki-Heck reaction. / Hirai, Go; Oguri, Hiroki; Moharram, Sameh M.; Koyama, Koji; Hirama, Masahiro.

In: Tetrahedron Letters, Vol. 42, No. 33, 13.08.2001, p. 5783-5787.

Research output: Contribution to journalArticle

Hirai, Go ; Oguri, Hiroki ; Moharram, Sameh M. ; Koyama, Koji ; Hirama, Masahiro. / Convergent synthesis of the ABC-ring moiety of zoanthenol : Intramolecular Mizoroki-Heck reaction. In: Tetrahedron Letters. 2001 ; Vol. 42, No. 33. pp. 5783-5787.
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