Bronsted acid-catalyzed aza Diels-Alder reaction of Danishefsky's diene with aldimine generated in situ from aldehyde and amine in aqueous media

被引：86

作者：

Akiyama, T ^{[1
]}

Takaya, J ^{[1
]}

Kagoshima, H ^{[1
]}

机构：

[1] Gakushuin Univ, Fac Sci, Dept Chem, Toshima Ku, Tokyo 1718588, Japan

来源：

TETRAHEDRON LETTERS | 1999年 / 40卷 / 44期

关键词：

aza Diels-Alder reaction; Danishefsky's diene; Bronsted acid; imines; aqueous media;

D O I：

10.1016/S0040-4039(99)01630-5

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Three-component aza Diels-Alder reaction, starting from aldehyde, aniline, and Danishefsky's diene, took place smoothly under the influence of HBF4 in aqueous media to afford dihydro-4-pyridone derivatives in high yields. (C) 1999 Elsevier Science Ltd. All rights reserved.

引用

页码：7831 / 7834

页数：4

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