A new entry to Amaryllidaceae alkaloids from carbohydrates: Total synthesis of (+)-vittatine

Masahiro Bohno; Hidetomo Imase; Noritaka Chida

doi:10.1039/b402762k

A new entry to Amaryllidaceae alkaloids from carbohydrates: Total synthesis of (+)-vittatine

Masahiro Bohno, Hidetomo Imase, Noritaka Chida

応用化学科

研究成果: Article › 査読

33 被引用数 (Scopus)

抄録

The stereoselective and chiral synthesis of the Amaryllidaceae alkaloid, (+)-vittatine 1, is described; the quaternary carbon in 1 was generated by Claisen rearrangement of a cyclohexenol derived from D-glucose by way of a Ferrier's carbocyclisation reaction and a hexahydroindole skeleton was effectively constructed by intramolecular aminomercuration-demercuration, followed by Chugaev reaction.

本文言語	English
ページ（範囲）	1086-1087
ページ数	2
ジャーナル	Chemical Communications
巻	4
号	9
DOI	https://doi.org/10.1039/b402762k
出版ステータス	Published - 2004

ASJC Scopus subject areas

触媒
電子材料、光学材料、および磁性材料
セラミックおよび複合材料
化学 (全般)
表面、皮膜および薄膜
金属および合金
材料化学

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AU - Chida, Noritaka

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A new entry to Amaryllidaceae alkaloids from carbohydrates: Total synthesis of (+)-vittatine

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