| Literature DB >> 30398359 |
Mahboobeh Azizi1, Mahboobeh Nasr-Esfahani1, Iraj Mohammadpoor-Baltork1, Majid Moghadam1, Valiollah Mirkhani1, Shahram Tangestaninejad1, Reza Kia2.
Abstract
This report explains an efficient method for synthesis of an array of quinolines via the reaction of 2-aminoaryl ketones with terminal and internal alkynes in the presence of propylphosphonium tetrachloroindate ionic liquid supported on nanosilica (PPInCl-nSiO2) as a heterogeneous and reusable catalyst under solvent-free conditions. Inspired by this catalytic system, the first easy one-step synthesis of symmetric and unsymmetric pyrido[3,2- g or 2,3- g]quinolines was investigated through the reaction of diaroylphenylenediamines with one alkyne or two different alkynes.Entities:
Year: 2018 PMID: 30398359 DOI: 10.1021/acs.joc.8b02261
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354