Diastereoselective iodocarbocyclization reaction of 8-phenylmenthyl allylmalonate: An efficient preparation of a synthetic intermediate of cyclopropane amino acids

Tadashi Inoue; Osamu Kitagawa; Orie Ochiai; Takeo Taguchi

doi:10.1016/0957-4166(95)00063-U

Diastereoselective iodocarbocyclization reaction of 8-phenylmenthyl allylmalonate: An efficient preparation of a synthetic intermediate of cyclopropane amino acids

Tadashi Inoue, Osamu Kitagawa, Orie Ochiai, Takeo Taguchi

研究成果: Article › 査読

27 被引用数 (Scopus)

抄録

The iodocarbocyclization of allylmalonate using (-)-8-phenylmenthol as a chiral auxiliary proceeded with high diastereoselectivity to give the iodomethylcyclopropane dicarboxylic ester in good yield.

本文言語	English
ページ（範囲）	691-692
ページ数	2
ジャーナル	Tetrahedron: Asymmetry
巻	6
号	3
DOI	https://doi.org/10.1016/0957-4166(95)00063-U
出版ステータス	Published - 1995 3月
外部発表	はい

ASJC Scopus subject areas

触媒
物理化学および理論化学
有機化学
無機化学

文献へのアクセス

10.1016/0957-4166(95)00063-U

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引用スタイル

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abstract = "The iodocarbocyclization of allylmalonate using (-)-8-phenylmenthol as a chiral auxiliary proceeded with high diastereoselectivity to give the iodomethylcyclopropane dicarboxylic ester in good yield.",

author = "Tadashi Inoue and Osamu Kitagawa and Orie Ochiai and Takeo Taguchi",

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AU - Taguchi, Takeo

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