| Literature DB >> 28357867 |
Rongrong Yu1, Xingyu Chen1, Stephen F Martin2, Zhiqian Wang1.
Abstract
A new route to phosphines was developed by a method that features a "pre-join and transform" process that proceeds via acylphosphine intermediates that may be readily prepared from carboxylic acids and disubstituted phosphines. The efficient decarbonylations of these acylphosphines using a nickel catalyst delivered the corresponding phosphines. This method shows that the carboxyl group can play a role similar to halides or triflates for introducing a substituted phosphorus atom on an aromatic ring.Entities:
Year: 2017 PMID: 28357867 DOI: 10.1021/acs.orglett.7b00579
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005