Issue 53, 2019

Palladium(ii)-catalyzed synthesis of indenones through the cyclization of benzenecarbaldehydes with internal alkynes

Abstract

The palladium(II)-catalyzed carbocyclization of benzenecarbaldehydes with internal alkynes to afford 2,3-disubstituted indenones was reported. The annulation reaction proceeded through the transmetalation of Pd(II) with an aromatic aldehyde and the insertion of internal alkynes, followed by cyclization via the intramolecular nucleophilic addition of intermediate organopalladium(II) species to the aldehyde group. This reaction proceeded in moderate to good yields with high regioselectivity.

Graphical abstract: Palladium(ii)-catalyzed synthesis of indenones through the cyclization of benzenecarbaldehydes with internal alkynes

Supplementary files

Article information

Article type
Paper
Submitted
24 May 2019
Accepted
15 Sep 2019
First published
02 Oct 2019
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2019,9, 31162-31168

Palladium(II)-catalyzed synthesis of indenones through the cyclization of benzenecarbaldehydes with internal alkynes

J. Kashanna, R. Aravind Kumar and R. Kishore, RSC Adv., 2019, 9, 31162 DOI: 10.1039/C9RA03921J

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