Alkenylation of arenes using disubstituted ethynes by palladium/carboxylic acid catalysis

15Citations
Citations of this article
6Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Palladium/carboxylic acid-catalyzed alkenylation of heteroarenes and electron-deficient arenes using alkynes underwent C(sp2)H bond activation in arene substrates to give the corresponding alkenylarenes straightforwardly. The versatility of this transformation is demonstrated by the double alkenylation of functionalized thiophenes and 5,6-difluorobenzothiadiazole with alkynes and provides a one-step access to vinylenearylene- vinylene units.

Author supplied keywords

Cite

CITATION STYLE

APA

Minami, Y., Furuya, Y., Kodama, T., & Hiyama, T. (2018). Alkenylation of arenes using disubstituted ethynes by palladium/carboxylic acid catalysis. Chemistry Letters, 47(5), 674–677. https://doi.org/10.1246/cl.180143

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free