Ionic liquid promoted aza-Diels-Alder reaction of Danishefsky's diene with imines

被引：18

作者：

Pégot, B ^{[1
]}

Vo-Thanh, G ^{[1
]}

机构：

[1] Univ Paris 11, ICMMO, Lab React Select Supports, CNRS UMR 8615, F-91405 Orsay, France

来源：

SYNLETT | 2005年 / 09期

关键词：

ionic liquids; aza-Diels-Alder reaction; Danishefsky's diene; imines; green chemistry;

D O I：

10.1055/s-2005-869837

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A highly efficient procedure for the synthesis of 2-substituted-2,3-dihydro-4-pridone derivatives through the aza-Diels-Alder reaction under 'green chemistry' conditions is described. The reaction of Danishefsky's diene with imines has been found to perform better at room temperature in ionic liquids without an acid catalyst and organic solvent: the ionic liquids are recycled while their efficiency is preserved.

引用

页码：1409 / 1412

页数：4

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