Recent advances of propiolic acids in organic reactions

被引：30
作者：
Chen, Chuanli [1 ]
Wu, Jinjing [1 ]
Yan, Guobing [1 ]
Huang, Dayun [1 ]
机构：
[1] Lishui Univ, Dept Chem, 1 Xueyuan Rd, Lishui City 323000, Zhejiang, Peoples R China
来源：
TETRAHEDRON LETTERS | 2020年 / 61卷 / 04期
关键词：
Mechanism; Decarboxylative; Nucleophile; Electrophilie; ALKYNYL CARBOXYLIC-ACIDS; DECARBOXYLATIVE COUPLING REACTIONS; ONE-POT SYNTHESIS; DIASTEREOSELECTIVE TOTAL-SYNTHESIS; UGI INTRAMOLECULAR HYDROARYLATION; H-PHOSPHINE OXIDES; MICROWAVE-ASSISTED SYNTHESIS; DIVERSITY-ORIENTED SYNTHESIS; CATALYZED DIRECT SYNTHESIS; METAL-FREE APPROACH;
D O I：
10.1016/j.tetlet.2019.151415
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
Herein, recent advances of propiolic acids in decade (2009-2019) were summarized as five pathways according to their triggered mechanisms: (1) acids as nucleophiles; (2) electrophilic alkynes; (3) decarboxylative coupling; (4) decarboxylative addition; (5) electrophilic acids. Reactions with alkenes, alkynes, isocyanides, indonium, free radicals, R-X (X = leaving groups) et al were discussed. We hope this review will promote future research in this area. (C) 2019 Elsevier Ltd. All rights reserved.
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页数：16
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