A new approach to asymmetric synthesis of Stork's prostaglandin intermediate

Makoto Nakazawa, Yasuharu Sakamoto, Takashi Takahashi, Katsuhiko Tomooka, Katsuya Ishikawa, Takeshi Nakai

Research output: Contribution to journalArticle

20 Citations (Scopus)

Abstract

A stereocontrolled approach to assymmetric synthesis of Stork's prostaglandin intermediate 3 has been developed which involves the [2,3]-Wittig rearrangement and the Pd(II)-catalyzed allylic acetate rearrangement as the key steps.

Original languageEnglish
Pages (from-to)5923-5926
Number of pages4
JournalTetrahedron Letters
Volume34
Issue number37
DOIs
Publication statusPublished - Sep 10 1993
Externally publishedYes

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Prostaglandins
Acetates

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

Cite this

A new approach to asymmetric synthesis of Stork's prostaglandin intermediate. / Nakazawa, Makoto; Sakamoto, Yasuharu; Takahashi, Takashi; Tomooka, Katsuhiko; Ishikawa, Katsuya; Nakai, Takeshi.

In: Tetrahedron Letters, Vol. 34, No. 37, 10.09.1993, p. 5923-5926.

Research output: Contribution to journalArticle

Nakazawa, M, Sakamoto, Y, Takahashi, T, Tomooka, K, Ishikawa, K & Nakai, T 1993, 'A new approach to asymmetric synthesis of Stork's prostaglandin intermediate', Tetrahedron Letters, vol. 34, no. 37, pp. 5923-5926. https://doi.org/10.1016/S0040-4039(00)73815-9
Nakazawa, Makoto ; Sakamoto, Yasuharu ; Takahashi, Takashi ; Tomooka, Katsuhiko ; Ishikawa, Katsuya ; Nakai, Takeshi. / A new approach to asymmetric synthesis of Stork's prostaglandin intermediate. In: Tetrahedron Letters. 1993 ; Vol. 34, No. 37. pp. 5923-5926.
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