Bifunctional ligand enabled selective alkoxycarbonylation of aliphatic alkenes

Abstract
Carbazole derived phosphine ligands containing pyridine moiety were designed and prepared. It allows the challenging Pd-catalyzed Markovnikov-selective alkoxycarbonylation of aliphatic alkenes to give the branched ester products (28 examples; 51-97% branch selectivity). Preliminary mechanistic studies sup-port that the bridging bromide between Pd and Mn centers is crucial for the enhancement of regioselectivity. (c) 2022 Elsevier Inc. All rights reserved.

Keywords Plus:PALLADIUM-CATALYZED ALKOXYCARBONYLATIONBIMETALLIC CATALYSISCARBONYLATIONCOMPLEXESMETHOXYCARBONYLATIONHYDROXYCARBONYLATIONMECHANISMHYDROESTERIFICATIONSTYRENEREGIOSELECTIVITY

Published in JOURNAL OF CATALYSIS,Volume409;10.1016/j.jcat.2022.03.029,MAY 2022

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