Highly periselective [2,3]wittig rearrangements on dihydrofuran and dihydropyran rings

Katsuhiko Tomooka, Masashi Watanabe, Takeshi Nakai

Research output: Contribution to journalArticle

10 Citations (Scopus)

Abstract

The carbanion 3,5-arrangements involving the dihydrofuran and dihydropyran rings as migrating groups are shown to afford exclusively the [2,3]Wittig products with a remarkably high periselectivity and stereoselectivity.

Original languageEnglish
Pages (from-to)7353-7354
Number of pages2
JournalTetrahedron Letters
Volume31
Issue number50
DOIs
Publication statusPublished - 1990
Externally publishedYes

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Stereoselectivity

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

Cite this

Highly periselective [2,3]wittig rearrangements on dihydrofuran and dihydropyran rings. / Tomooka, Katsuhiko; Watanabe, Masashi; Nakai, Takeshi.

In: Tetrahedron Letters, Vol. 31, No. 50, 1990, p. 7353-7354.

Research output: Contribution to journalArticle

Tomooka, Katsuhiko ; Watanabe, Masashi ; Nakai, Takeshi. / Highly periselective [2,3]wittig rearrangements on dihydrofuran and dihydropyran rings. In: Tetrahedron Letters. 1990 ; Vol. 31, No. 50. pp. 7353-7354.
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