Issue 13, 2021

Palladium-catalyzed gaseous CO-free carbonylative C–C bond activation of cyclobutanones

Abstract

A palladium-catalyzed carbonylative C–C bond activation reaction of cyclobutanones proceeding by C–C bond cleavage, ring-opening, and amino- or alkoxycarbonylation is reported here. Two C–C bonds and one C–O or C–N bond are created to afford a variety of indanones bearing ester or amide groups under gas-free conditions by using phenyl formate and benzene-1,3,5-triyl triformate (TFBen) as convenient CO surrogates.

Graphical abstract: Palladium-catalyzed gaseous CO-free carbonylative C–C bond activation of cyclobutanones

Supplementary files

Article information

Article type
Research Article
Submitted
25 Mar 2021
Accepted
24 Apr 2021
First published
26 Apr 2021

Org. Chem. Front., 2021,8, 3398-3403

Palladium-catalyzed gaseous CO-free carbonylative C–C bond activation of cyclobutanones

K. Song, B. Wu, W. Gan, W. Yang, X. Chen, J. Cao and L. Xu, Org. Chem. Front., 2021, 8, 3398 DOI: 10.1039/D1QO00467K

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