Bronsted acid-catalyzed aza Diels-Alder reaction of Danishefsky's diene with aldimine generated in situ from aldehyde and amine in aqueous media
Bronsted acid-catalyzed aza Diels-Alder reaction of Danishefsky's diene with aldimine generated in situ from aldehyde and amine in aqueous media
复制标题
DOI：
10.1016/s0040-4039(99)01630-5
复制
发表时间：
1999-10-29
影响因子：
1.8
通讯作者：
Kagoshima, H
中科院分区：
文献类型：
--
作者：
Akiyama, T;Takaya, J;Kagoshima, H
在HBF4的作用下，以醛、苯胺和Danishefsky's diene为起始原料，在水溶液中顺利进行了三组分aza Diels-Alder反应，得到了高产率的4-吡啶二氢衍生物。1999爱思唯尔科学有限公司版权所有。
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.