How Can High Diastereoselectivity Be Attained in the Michael Addition of Ketene Silyl Acetals?

Junzo Otera; Yukihiro Fujita; Tsuneo Sato; Hitosi Nozaki; Shunichi Fukuzumi; Morifumi Fujita

doi:10.1021/jo00045a005

How Can High Diastereoselectivity Be Attained in the Michael Addition of Ketene Silyl Acetals?

Junzo Otera, Yukihiro Fujita, Tsuneo Sato, Hitosi Nozaki, Shunichi Fukuzumi, Morifumi Fujita

Department of Chemistry & Nanoscience

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

23 Scopus citations

Abstract

Criteria for attaining high diastereoselectivity in the title reaction are elucidated in terms of suppressing an electron-transfer process.

Original language	English
Pages (from-to)	5054-5055
Number of pages	2
Journal	Journal of Organic Chemistry
Volume	57
Issue number	19
DOIs	https://doi.org/10.1021/jo00045a005
State	Published - 1 Sep 1992

Access to Document

10.1021/jo00045a005

Cite this

@article{f32cb98052b94ab3bb459c257066485c,

title = "How Can High Diastereoselectivity Be Attained in the Michael Addition of Ketene Silyl Acetals?",

abstract = "Criteria for attaining high diastereoselectivity in the title reaction are elucidated in terms of suppressing an electron-transfer process.",

author = "Junzo Otera and Yukihiro Fujita and Tsuneo Sato and Hitosi Nozaki and Shunichi Fukuzumi and Morifumi Fujita",

year = "1992",

month = sep,

day = "1",

doi = "10.1021/jo00045a005",

language = "English",

volume = "57",

pages = "5054--5055",

journal = "Journal of Organic Chemistry",

issn = "0022-3263",