Transition metal-catalyzed reactions of propargylic carboxylates via an initial 1,2-acyloxy migration

被引:16
|
作者
Wang, Shaozhong [1 ]
机构
[1] Nanjing Univ, Sch Chem & Chem Engn, Jiangsu Key Lab Adv Organ Mat, State Key Lab Coordinat Chem, Nanjing 210023, Jiangsu, Peoples R China
基金
美国国家科学基金会;
关键词
Transition metal; 1,2-Acyloxy migration; Propargylic carboxylate; Carbenoid; Cycloaddition; MIGRATION/INTRAMOLECULAR 3+2 CYCLOADDITION; FACE-SELECTIVE PLATINUM; GOLD CATALYSIS; CHIRALITY TRANSFER; RAUTENSTRAUCH REARRANGEMENT; MECHANISTIC INSIGHTS; NAZAROV CYCLIZATION; TANDEM 1,2-ACYLOXY; ENYNYL ESTERS; CYCLOISOMERIZATION;
D O I
10.1016/j.tetlet.2018.02.054
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Propargylic carboxylates, as a type of easily available alkyne compounds, have attracted considerable attentions in recent decade. Under the catalysis of transition metal complex (Pd, Ru, Pt, Au, Rh etc), one of chemical transformations of propargylic carboxylate is 1,2-acyloxy migration. The resultant alkenyl metallocarbenoid or metal-containing species may undergo a variety of chemical transformations, leading to formation of carbocyclic and heterocyclic compounds. In this review, representative domino reactions initiated by 1,2-acyloxy migration of propargylic carboxylates are summarized, including pentannuations, cycloadditions and rearrangements. Some mechanistic discussions and synthetic applications are also included. (C) 2018 Elsevier Ltd, All rights reserved.
引用
收藏
页码:1317 / 1327
页数:11
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