Asymmetric double aldol reaction of chiral acetyloxazolidinone

Hiroshi Furuno; Tadashi Inoue; Atsushi Abiko

doi:10.1016/S0040-4039(02)02021-X

Asymmetric double aldol reaction of chiral acetyloxazolidinone

Hiroshi Furuno, Tadashi Inoue, Atsushi Abiko

研究成果: Contribution to journal › Article › 査読

17 被引用数 (Scopus)

抄録

Treatment of chiral oxazolidinone with Bu₂BOTf (2.5 equiv.) and Et₃N (3.0 equiv.) quantitatively produced the doubly borylated enolate, which afforded the double aldol products with high diastereoselectivity after reaction with aldehydes.

本文言語	英語
ページ（範囲）	8297-8299
ページ数	3
ジャーナル	Tetrahedron Letters
巻	43
号	46
DOI	https://doi.org/10.1016/S0040-4039(02)02021-X
出版ステータス	出版済み - 11 11 2002

All Science Journal Classification (ASJC) codes

Biochemistry
Drug Discovery
Organic Chemistry

文献へのアクセス

10.1016/S0040-4039(02)02021-X

フィンガープリント「Asymmetric double aldol reaction of chiral acetyloxazolidinone」の研究トピックを掘り下げます。これらがまとまってユニークなフィンガープリントを構成します。

引用スタイル

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title = "Asymmetric double aldol reaction of chiral acetyloxazolidinone",

abstract = "Treatment of chiral oxazolidinone with Bu2BOTf (2.5 equiv.) and Et3N (3.0 equiv.) quantitatively produced the doubly borylated enolate, which afforded the double aldol products with high diastereoselectivity after reaction with aldehydes.",

author = "Hiroshi Furuno and Tadashi Inoue and Atsushi Abiko",

note = "Funding Information: This work was supported by a grant from the Ministry of Education, Culture, Sports, Science and Technology of Japan (Grant-in-Aid 10640578 and 13640533). ",

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AU - Furuno, Hiroshi

AU - Inoue, Tadashi

AU - Abiko, Atsushi

N1 - Funding Information: This work was supported by a grant from the Ministry of Education, Culture, Sports, Science and Technology of Japan (Grant-in-Aid 10640578 and 13640533).

PY - 2002/11/11

Y1 - 2002/11/11

N2 - Treatment of chiral oxazolidinone with Bu2BOTf (2.5 equiv.) and Et3N (3.0 equiv.) quantitatively produced the doubly borylated enolate, which afforded the double aldol products with high diastereoselectivity after reaction with aldehydes.

AB - Treatment of chiral oxazolidinone with Bu2BOTf (2.5 equiv.) and Et3N (3.0 equiv.) quantitatively produced the doubly borylated enolate, which afforded the double aldol products with high diastereoselectivity after reaction with aldehydes.

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