4.4 Article

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

期刊

TETRAHEDRON LETTERS
卷 59, 期 14, 页码 1317-1327

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2018.02.054

关键词

Transition metal; 1,2-Acyloxy migration; Propargylic carboxylate; Carbenoid; Cycloaddition

资金

  1. National Science Foundation of China [20802034, 21572098]
  2. Natural Science Foundation of Jiangsu Province [BK 2009229, BK 20141313]

向作者/读者索取更多资源

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.

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