A Concise enantioselective synthesis of acromelic acid B from (S)-O-benzylglycidol

Seiichi Takano; Shun'ichi Tomita; Yoshiharu Iwabuchi; Kunio Ogasawara

doi:10.3987/COM-89-5064

A Concise enantioselective synthesis of acromelic acid B from (S)-O-benzylglycidol

Seiichi Takano, Shun'ichi Tomita, Yoshiharu Iwabuchi, Kunio Ogasawara

PHA - Molecular Pharmaceutical Science

Research output: Contribution to journal › Article › peer-review

32 Citations (Scopus)

Abstract

The potent neurotoxin, acromelic acid B, has been synthesized by an enantioselective route employing an intramolecular 1,3-dipolar cyclization as the key step.

Original language	English
Pages (from-to)	1473-1476
Number of pages	4
Journal	Heterocycles
Volume	29
Issue number	8
DOIs	https://doi.org/10.3987/COM-89-5064
Publication status	Published - 1989 Aug 1

ASJC Scopus subject areas

Analytical Chemistry
Pharmacology
Organic Chemistry

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title = "A Concise enantioselective synthesis of acromelic acid B from (S)-O-benzylglycidol",

abstract = "The potent neurotoxin, acromelic acid B, has been synthesized by an enantioselective route employing an intramolecular 1,3-dipolar cyclization as the key step.",

author = "Seiichi Takano and Shun'ichi Tomita and Yoshiharu Iwabuchi and Kunio Ogasawara",

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AU - Ogasawara, Kunio

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ER -

A Concise enantioselective synthesis of acromelic acid B from (S)-O-benzylglycidol

Abstract

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