A versatile synthetic method for preparing 1,2,3,5-tetrasubstituted pyrroles using isothiocyanates and 2-alkynyl ethers or 2-alkynylamines as building units

被引：0
|
作者：
Brandsma, L
Nedolya, NA
Trofimov, BA
机构：
[1] Univ Utrecht, Debye Inst, Dept Preparat Organ Chem, NL-3584 CH Utrecht, Netherlands
[2] Russian Acad Sci, Inst Chem, Siberian Branch, RUS-664033 Irkutsk, Russia
来源：
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY | 1999年 / 1999卷 / 10期
关键词：
metallations; copper; homogeneous catalysis; cyclizations; regioselectivity; azatrienes;
D O I：
暂无
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
A fundamentally new approach for the construction of pyrrole rings is exemplified by highly efficient one-pot syntheses of 1,2,3,5-tetrasubstituted pyrroles starting from alkyl isothiocyanates and 2-alkynylamines or 2-alkynyl ethers.
引用
收藏
页码：2663 / 2664
页数：2
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