Tandem Diels-Alder cyclization/aromatization reactions of 5-vinyl-1-acyl-2-aryl-2,3-dihydro-4-pyridones

被引：10

作者：

Kuethe, JT ^{[1
]}

Comins, DL ^{[1
]}

机构：

[1] N Carolina State Univ, Dept Chem, Raleigh, NC 27695 USA

来源：

TETRAHEDRON LETTERS | 2003年 / 44卷 / 22期

基金：

美国国家卫生研究院; 美国国家科学基金会;

关键词：

D O I：

10.1016/S0040-4039(03)00930-4

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A tandem Diels-Alder cyclization/aromatization of 5-vinyl-2,3-dihydro-4-pyridones and various dienophiles is reported. The intermediate Diels-Alder cycloadduct undergoes an elimination/aromatization to provide beta-amino-ketones, beta-amino-alcohols, and unnatural amino acids containing useful functionality. (C) 2003 Elsevier Science Ltd. All rights reserved.

引用

页码：4179 / 4182

页数：4

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