Issue 24, 2019

A gold-catalyzed facile intramolecular rearrangement and cyclization sequence for synthesis of 2,5-dihydrofurans

Abstract

An efficient gold-catalyzed intramolecular rearrangement and cyclization protocol was developed for synthesis of 2,5-dihydrofuran derivatives from O-propargyl β-enaminones. In this organic transformation new C–C and C–O bonds are formed under mild reaction conditions; this includes the formation of a quaternary centre.

Graphical abstract: A gold-catalyzed facile intramolecular rearrangement and cyclization sequence for synthesis of 2,5-dihydrofurans

Supplementary files

Article information

Article type
Paper
Submitted
02 Apr 2019
Accepted
14 May 2019
First published
14 May 2019

Org. Biomol. Chem., 2019,17, 6015-6024

A gold-catalyzed facile intramolecular rearrangement and cyclization sequence for synthesis of 2,5-dihydrofurans

K. Sunil, Y. Thummala, P. Dalovai, S. Balasubramanian and G. V. Karunakar, Org. Biomol. Chem., 2019, 17, 6015 DOI: 10.1039/C9OB00756C

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