| Literature DB >> 31971802 |
Rachel M Shanahan1, Aobha Hickey1, Lorraine M Bateman1,2,3, Mark E Light4, Gerard P McGlacken1,2.
Abstract
Herein, we report a one-pot process that marries mechanistically distinct, traditional cross-coupling reactions with C-H functionalization using the same precatalyst. The reactions proceed in yields of up to 95%, in air, and require no extraneous ligand. The reactions are thought to be facilitated by harnessing the substrate quinoline as an N-ligand, and evidence of the palladium-quinoline interaction is provided by 1H-15N HMBC NMR spectroscopy and X-ray crystallographic structures. Application of the methodology is demonstrated by the quick formation of fluorescent, π-extended frameworks.Entities:
Year: 2020 PMID: 31971802 DOI: 10.1021/acs.joc.9b03321
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354