Issue 6, 2024

Towards tetrasubstituted furans through rearrangement and cyclodimerization of acetylenic ketones

Abstract

Cyclodimerization of readily accessible acetylenic ketones facilitated by a phosphane–borane complex under basic conditions is achieved. This methodology allows one-pot synthesis of phosphorus-involved tetrasubstituted furans via the construction of a C–P bond and a furan ring within a single procedure. A plausible reaction mechanism is proposed.

Graphical abstract: Towards tetrasubstituted furans through rearrangement and cyclodimerization of acetylenic ketones

Supplementary files

Article information

Article type
Communication
Submitted
14 Dec 2023
Accepted
09 Jan 2024
First published
11 Jan 2024

Org. Biomol. Chem., 2024,22, 1172-1175

Towards tetrasubstituted furans through rearrangement and cyclodimerization of acetylenic ketones

Z. Dai, C. Xu, R. Tian and Z. Duan, Org. Biomol. Chem., 2024, 22, 1172 DOI: 10.1039/D3OB02036C

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