| Literature DB >> 30779270 |
Jiawang Liu1, Ji Yang1, Francesco Ferretti1,2, Ralf Jackstell1, Matthias Beller1.
Abstract
The first catalyst for the alkoxycarbonylation of gem-difluoroalkenes is described. This novel catalytic transformation proceeds in the presence of Pd(acac)2 /1,2-bis((di-tert-butylphosphan-yl)methyl)benzene (btbpx) (L4) and allows for an efficient and straightforward access to a range of difluoromethylated esters in high yields and regioselectivities. The synthetic utility of the protocol is showcased in the practical synthesis of a Cyclandelate analogue using this methodology as the key step.Entities:
Keywords: carbonylation; difluoromethylated esters; fluoroalkenes; palladium; selectivity
Year: 2019 PMID: 30779270 DOI: 10.1002/anie.201813801
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336