1,4-Remote stereocontrol via asymmetric [2,3]-Wittig rearrangements

Katsuhiko Tomooka; Ping Huai Keong; Takeshi Nakai

doi:10.1016/0040-4039(95)00397-U

1,4-Remote stereocontrol via asymmetric [2,3]-Wittig rearrangements

Katsuhiko Tomooka, Ping Huai Keong, Takeshi Nakai

研究成果: Contribution to journal › Article › 査読

12 被引用数 (Scopus)

抄録

The carbanion rearrangement of the propargylic ether of the β-(1-alkoxyethyl) allyl alcohol was found to proceed with a high degree of either 1,4-syn or 1,4-anti selection by virtue of the proper choice of the combination of the alkoxy group with the solvent used.

本文言語	英語
ページ（範囲）	2789-2792
ページ数	4
ジャーナル	Tetrahedron Letters
巻	36
号	16
DOI	https://doi.org/10.1016/0040-4039(95)00397-U
出版ステータス	出版済み - 4 17 1995
外部発表	はい

All Science Journal Classification (ASJC) codes

Biochemistry
Drug Discovery
Organic Chemistry

文献へのアクセス

10.1016/0040-4039(95)00397-U

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引用スタイル

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abstract = "The carbanion rearrangement of the propargylic ether of the β-(1-alkoxyethyl) allyl alcohol was found to proceed with a high degree of either 1,4-syn or 1,4-anti selection by virtue of the proper choice of the combination of the alkoxy group with the solvent used.",

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