1,3-Dipolar cycloaddition reactions of azomethine ylides and alkynes

被引：34
|
作者：
Gulevskaya, Anna V. [1 ]
Nelina-Nemtseva, Julia I. [1 ]
机构：
[1] Southern Fed Univ, Fac Chem, 7 Zorge St, Rostov Na Donu 344090, Russia
来源：
CHEMISTRY OF HETEROCYCLIC COMPOUNDS | 2018年 / 54卷 / 12期
关键词：
alkynes; azomethine ylides; fused pyrroles; pyrroles; 1,3-dipolar cycloaddition; 2-ETHYNYLPYRIDINE N-YLIDES; SUBSTITUTED INDOLIZINES; STEREOSELECTIVE-SYNTHESIS; ACID-CHLORIDES; INTRAMOLECULAR CYCLIZATION; ENANTIOSELECTIVE SYNTHESIS; ACETYLENIC DIPOLAROPHILES; ALPHA-SILYLIMINES; L-PROLINE; ONE-POT;
D O I：
10.1007/s10593-019-02398-5
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
In this review, we consider 1,3-dipolar cycloaddition reactions between azomethine ylides and alkynes, resulting in the formation of pyrroles, as well as their hydrogenated and fused analogs. The references have been arranged according to the types of azomethine ylides and the methods used for their generation. The review is mainly focused on literature sources published since year 2000 and contains 133 references.
引用
收藏
页码：1084 / 1107
页数：24
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