Dienophilic reactivity of perfluoroalkenyl ketones in Diels-Alder reactions

被引：25

作者：

Chanteau, F

Essers, M

Plantier-Royon, R

Haufe, G

Portella, C

机构：

[1] Univ Reims, Fac Sci, CNRS, UMR 6519,Lab React Select & Applicat, F-51687 Reims 2, France

[2] Univ Munster, Inst Organ Chem, D-48149 Munster, Germany

来源：

TETRAHEDRON LETTERS | 2002年 / 43卷 / 09期

关键词：

Diels-Alder reactions; enones; perfluoroalkenyl compounds; organofluorine;

D O I：

10.1016/S0040-4039(02)00107-7

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Perfluoroalkenyl ketones, obtained by reaction of perfluoroorganometallic reagents with acylsilanes, are shown to be versatile dienophiles in Diels-Alder reactions with various dienes. (C) 2002 Elsevier Science Ltd. All rights reserved.

引用

页码：1677 / 1680

页数：4

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