Impact Factor:4.5

DOI number:10.1039/d0qo01203c

Journal:Organic Chemistry Frontiers

Abstract:Palladium-catalyzed alkoxycarbonylation reactions allow for the efficient conversion of widely available unsaturated compounds, CO and alcohols into the corresponding carboxylic acid derivatives. A driving force for the development of new and improved catalytic methodologies is the design and synthesis of ligands, which fine-tune the properties of the metal center. In general, alternation of the ligand backbone and substituents adjusts the electronic and steric properties of the active catalyst species to control activity and selectivity of a given catalytic process. Therefore, our group has a long-standing interest in ligand developments. In the past decade, several classes of ligands have been developed by us for palladium-catalyzed carbonylation reactions, which are summarized in this article. As an example, mono- and bidentate phosphines with heteroaromatic backbones were prepared to overcome the limitations of known catalyst systems. The common feature of all these ligands is the function of the integrated base, which acts as a proton shuttle for the formation of the palladium hydride and the rate-determining N-assisted alcoholysis. On the other hand, the basic substituent improves the durability of the catalyst via hemilabile coordination to the palladium center in the catalytic cycle.

Co-author:Ralf Jackstell；Robert Franke；Matthias Beller*

First Author:Rui Sang；Yuya Hu；Rauf Razzaq

Indexed by:Journal paper

Correspondence Author:Matthias Beller*

Document Type:J

Volume:8

Issue:4

Page Number:799-811

Translation or Not:no

Date of Publication:2021-02-21

Included Journals:SCI

Links to published journals:https://pubs.rsc.org/en/content/articlelanding/2021/qo/d0qo01203c