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

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

doi:10.1016/S0040-4039(00)73815-9

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 journal › Article › peer-review

21 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 language	English
Pages (from-to)	5923-5926
Number of pages	4
Journal	Tetrahedron Letters
Volume	34
Issue number	37
DOIs	https://doi.org/10.1016/S0040-4039(00)73815-9
Publication status	Published - Sept 10 1993
Externally published	Yes

All Science Journal Classification (ASJC) codes

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/S0040-4039(00)73815-9

Cite this

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title = "A new approach to asymmetric synthesis of Stork's prostaglandin intermediate",

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.",

author = "Makoto Nakazawa and Yasuharu Sakamoto and Takashi Takahashi and Katsuhiko Tomooka and Katsuya Ishikawa and Takeshi Nakai",

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AU - Nakazawa, Makoto

AU - Sakamoto, Yasuharu

AU - Takahashi, Takashi

AU - Tomooka, Katsuhiko

AU - Ishikawa, Katsuya

AU - Nakai, Takeshi

PY - 1993/9/10

Y1 - 1993/9/10

N2 - 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.

AB - 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.

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DO - 10.1016/S0040-4039(00)73815-9

M3 - Article

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JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 37

ER -

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

Abstract

All Science Journal Classification (ASJC) codes

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