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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.

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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, Accepted Manuscript

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

    G. V. karunakar, K. Sunil, Y. Thummala, P. Dalovai and S. Balasubramanian, Org. Biomol. Chem., 2019, Accepted Manuscript , DOI: 10.1039/C9OB00756C

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