| Literature DB >> 29528637 |
Rui Sang1, Peter Kucmierczyk1,2, Kaiwu Dong1, Robert Franke2,3, Helfried Neumann1, Ralf Jackstell1, Matthias Beller1.
Abstract
A general and selective palladium-catalyzed alkoxycarbonylation of all kinds of alkenes with formic acid (HCOOH, FA) is described. Terminal, di-, tri-, and tetra-substituted including functionalized olefins are converted into linear esters with high yields and regioselectivity. Key-to-success is the use of specific palladium catalysts containing ligands with built-in base, e.g., L5. Comparison experiments demonstrate that the active catalyst system not only facilitates isomerization and carbonylation of alkenes but also promotes the selective decomposition of HCOOH to CO under mild conditions.Entities:
Year: 2018 PMID: 29528637 DOI: 10.1021/jacs.8b01123
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419