| Literature DB >> 29874086 |
Yuto Okugawa1, Yoshihiro Hayashi2, Susumu Kawauchi2, Koji Hirano1, Masahiro Miura1.
Abstract
A diphosphination of arynes with diphosphines has been developed. The reaction of stable aryne precursors, 2-(trimethylsilyl)aryl triflates, with tetraaryldiphosphines proceeds in the presence of fluorine- or carbonate-based activators to deliver the corresponding diphosphinated products, sterically and electronically tuned 1,2-bis(diphenylphosphino)benzene (dppbz) derivatives, which can find wide application in transition metal catalysis and material science. Additionally, preliminary computational studies on the reaction mechanism are also reported.Entities:
Year: 2018 PMID: 29874086 DOI: 10.1021/acs.orglett.8b01470
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005