Jump to main content
Jump to site search

Issue 24, 2019
Previous Article Next Article

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

Author affiliations

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

Back to tab navigation

Supplementary files

Publication details

The article was received on 02 Apr 2019, accepted on 14 May 2019 and first published on 14 May 2019


Article type: Paper
DOI: 10.1039/C9OB00756C
Org. Biomol. Chem., 2019,17, 6015-6024

  •   Request permissions

    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

Search articles by author

Spotlight

Advertisements