CuBr2-catalyzed alkylation of furans with benzyl alcohols and benzaldehydes. Domino reactions including this alkylation as a key step

A CuBr2-catalyzed alkylation of furans with a broad scope of benzyl alcohols and benzaldehydes is reported. Reaction proceeds efficiently under mild reaction conditions requiring no inert atmosphere or other precautions. Moreover, it is shown that CuBr2 catalyzes domino reactions of furans with benzyl alcohols or benzaldehydes bearing a nucleophilic moiety in the ortho-position. These protocols offer a practical approach to densely substituted heterocyclic motifs from easily available furans. © 2017 Elsevier Ltd

Authors
Makarov A.S.1 , Kekhvaeva A.E.1 , Hall C.J.J.2 , Price D.R.2 , Trushkov I.V. 3, 4 , Uchuskin M.G. 1, 3
Journal
Number of issue
50
Language
English
Pages
7042-7053
Status
Published
Volume
73
Year
2017
Organizations
  • 1 Perm State University, Bukireva 15, Perm, 614990, Russian Federation
  • 2 University of Oxford, Chemistry Research Laboratory, Mansfield Road, Oxford, OX1 3TA, United Kingdom
  • 3 RUDN University, Miklukho-Maklaya 6, Moscow, 117198, Russian Federation
  • 4 Dmitry Rogachev National Research Center of Pediatric Hematology, Oncology and Immunology, Samory Mashela 1, Moscow, 117997, Russian Federation
Keywords
Benzofuran; CuBr2; Friedel-Crafts alkylation; Furan; Indole
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