Synthesis 2019; 51(18): 3410-3418
DOI: 10.1055/s-0037-1611567
paper
© Georg Thieme Verlag Stuttgart · New York

Palladium(II) Acetate Mediated Dimerization/Cycloisomerization of 2-Sulfonyl-4-alkynones: Synthesis of trans-1,2-Difurylethylenes

a   Department of Medicinal and Applied Chemistry, Kaohsiung Medical University, Kaohsiung 807, Taiwan
b   Department of Medical Research, Kaohsiung Medical University Hospital, Kaohsiung 807, Taiwan   Email: mychang@kmu.edu.tw
,
Kai-Xiang Lai
a   Department of Medicinal and Applied Chemistry, Kaohsiung Medical University, Kaohsiung 807, Taiwan
› Author Affiliations
The authors would like to thank the Ministry of Science and Technology of the People’s Republic of China for financial support (MOST 106-2628-M-037-001-MY3).
Further Information

Publication History

Received: 08 April 2019

Accepted after revision: 06 May 2019

Publication Date:
23 May 2019 (online)


Abstract

This paper describes a one-pot, atom-economic, easy-operation, open-atmosphere method for the synthesis of trans-1,2-difuryl­ethylenes by the straightforward Pd(OAc)2-mediated dimerization/cycloisomerization of 2-sulfonyl-4-alkynones in the presence of Na2CO3 and PPh3 under refluxing EtOH conditions, and proposes and discusses a plausible mechanism. This protocol provides a highly effective annulation via two carbon–oxygen (C–O) single-bond and one carbon–carbon (C=C) double-bond formations.

Supporting Information