Transition Metal-Catalyzed and Metal-Free Cyclization Reactions of Alkynes with Nitrogen-Containing Substrates: Synthesis of Pyrrole Derivatives

被引:42
|
作者
Neto, Jose S. S. [1 ]
Zeni, Gilson [2 ]
机构
[1] Univ Fed Santa Catarina, Dept Quim, Florianopolis 88040900, SC, Brazil
[2] Univ Fed Santa Maria, Dept Biochem & Mol Biol, Lab Sintese Reatividade Avaliacao Farmacol & Toxi, CCNE, Santa Maria 97105900, RS, Brazil
关键词
cyclization; pyrroles; alkynes; nitrogen source; catalysis; ONE-POT SYNTHESIS; HIGHLY SUBSTITUTED PYRROLES; PROPARGYLIC BETA-ENAMINONES; CHIRAL HOMOPROPARGYL SULFONAMIDES; GOLD(I)-CATALYZED TANDEM REACTION; INTERMOLECULAR NITRENE TRANSFER; PROMOTED 3-COMPONENT REACTION; ASYMMETRIC 2+2+2 CYCLIZATION; OXIDATIVE IPSO-ANNULATION; CONIA-ENE REACTION;
D O I
10.1002/cctc.201902325
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
This review describes the efforts in the synthesis of pyrrole derivatives using the reaction of alkynes with nitrogen-compounds under transition metal-catalyzed and metal-free conditions, in the past decade. We initially focused on the methods of preparation of pyrrole derivatives using reactions catalyzed by transition metal. In this part, we described the syntheses of 1-pyrrolines, 2-pyrrolines, 3-pyrrolines, pyrroles, and pyrrolidines following an alphabetical order of the transition metal used for the synthesis. Subsequently, we presented the synthesis of these pyrrole derivatives under metal-free conditions.
引用
收藏
页码:3335 / 3408
页数:74
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