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Title: Palladium-catalyzed chemoselective direct α-arylation of carbonyl compounds with chloroaryl triflates at the C-Cl site
Authors: Chen, Z 
Gu, C 
Yuen, OY 
So, CM 
Issue Date: 7-May-2022
Source: Chemical science, 7 May 2022, v. 13, no. 17, p. 4762-4769
Abstract: This study described palladium-catalyzed chemoselective direct α-arylation of carbonyl compounds with chloroaryl triflates in the Ar-Cl bond. The Pd/SelectPhos system showed excellent chemoselectivity toward the Ar-Cl bond in the presence of the Ar-OTf bond with a broad substrate scope and excellent product yields. The electronic and steric hindrance offered by the -PR2 group of the ligand with the C2-alkyl group was found to be the key factor affecting the reactivity and chemoselectivity of the α-arylation reaction. The chemodivergent approach was also successfully employed in the synthesis of flurbiprofen and its derivatives (e.g., -OMe and -F).
Publisher: Royal Society of Chemistry
Journal: Chemical science 
ISSN: 2041-6520
EISSN: 2041-6539
DOI: 10.1039/d1sc06701j
Rights: © 2022 The Author(s). Published by the Royal Society of Chemistry
This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence (https://creativecommons.org/licenses/by-nc/3.0/).
The following publication Chen, Z., Gu, C., Yuen, O. Y., & So, C. M. (2022). Palladium-catalyzed chemoselective direct α-arylation of carbonyl compounds with chloroaryl triflates at the C–Cl site. Chemical Science, 13(17), 4762-4769 is available at https://doi.org/10.1039/D1SC06701J.
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