Issue 89, 2016

Hypoiodite-catalysed oxidative cyclisation of Michael adducts of chalcones with 1,3-dicarbonyl compounds: a facile and versatile approach to substituted furans and cyclopropanes

Abstract

Through hypoiodite catalysis, oxidative cyclisation of Michael adducts of chalcones with 1,3-dicarbonyl compounds for divergent synthesis of either furans or cyclopropanes is developed. The selective synthesis of major products is achieved depending on the use of different reaction conditions or substrates.

Graphical abstract: Hypoiodite-catalysed oxidative cyclisation of Michael adducts of chalcones with 1,3-dicarbonyl compounds: a facile and versatile approach to substituted furans and cyclopropanes

Supplementary files

Article information

Article type
Communication
Submitted
11 Aug 2016
Accepted
11 Oct 2016
First published
11 Oct 2016

Chem. Commun., 2016,52, 13097-13100

Hypoiodite-catalysed oxidative cyclisation of Michael adducts of chalcones with 1,3-dicarbonyl compounds: a facile and versatile approach to substituted furans and cyclopropanes

W. Gao, F. Hu, J. Tian, X. Li, W. Wei and H. Chang, Chem. Commun., 2016, 52, 13097 DOI: 10.1039/C6CC06624K

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