Issue 9, 2024

Ru(ii)-catalyzed cascade cis carbohalogenation and cyclization of alkyne-tethered cyclohexadienones for synthesizing tetrasubstituted alkenes

Abstract

We have established an efficient ruthenium(II)-catalyzed cis carbohalogenation and carbooxygenation cyclization of internal alkyne-tethered cyclohexadienones with halide and acetate ions, which produces a series of alkenyl halides and acetates with hydrobenzofuran skeletons in high yields and features high atom economy and regio- and stereoselectivity. Furthermore, the obtained hydrobenzofuran products can easily undergo aromatization and subsequent cross-coupling reactions, which provide a novel and stereoselective approach to synthesize tetrasubstituted alkenes, particularly diarylalkenes and triarylalkenes.

Graphical abstract: Ru(ii)-catalyzed cascade cis carbohalogenation and cyclization of alkyne-tethered cyclohexadienones for synthesizing tetrasubstituted alkenes

Supplementary files

Article information

Article type
Research Article
Submitted
18 Jan 2024
Accepted
11 Mar 2024
First published
12 Mar 2024

Org. Chem. Front., 2024,11, 2572-2578

Ru(II)-catalyzed cascade cis carbohalogenation and cyclization of alkyne-tethered cyclohexadienones for synthesizing tetrasubstituted alkenes

X. Huang, C. Yi, R. Xiong, M. Bai, Y. Tang, S. Xu and Y. Li, Org. Chem. Front., 2024, 11, 2572 DOI: 10.1039/D4QO00105B

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