Fe3O4@SiO2—CPTMS—Guanidine—SO3H-catalyzed One-Pot Multicomponent Synthesis of Polysubstituted Pyrrole Derivatives under Solvent-Free Conditions
作者:H. Rostami、L. Shiri
DOI:10.1134/s1070428019080207
日期:2019.8
A highly efficient procedure for the one-pot synthesis of polysubstituted pyrrole derivatives by the reaction between of aniline derivatives, beta-diketones or beta-ketoesters, and beta-nitrostyrene derivatives in the presence of Fe3O4@SiO2-CPTMS-guanidine-SO3H as a reusable magnetic nanocatalyst is reported. The magnetic nanocatalyst was prepared and fully characterized by FTIR spectroscopy, scanning electron microscopy, energy dispersive X-ray spectroscopy, X-ray diffraction analysis, thermogravimetric analysis, and vibrating sample magnetometry.
Three-component direct synthesis of substituted pyrroles from easily accessible chemical moieties using hypervalent iodine reagent
作者:Nikhil C. Jadhav、Prashant B. Jagadhane、Hemlata V. Patile、Vikas N. Telvekar
DOI:10.1016/j.tetlet.2013.04.014
日期:2013.6
A novel and simple three-component system has been developed to synthesize substituted pyrroles from corresponding amines and nitrostyrenes using (diacetoxyiodo)benzene at reflux temperature in ethanol. The good to excellent yields were obtained with different types of functional groups. (C) 2013 Elsevier Ltd. All rights reserved.
10.1016/j.jphotochem.2024.115863
作者:Ahmadi, Faezeh、Shariatipour, Monire、Jadidi Nejad, Masoumeh、Heydari, Akbar
DOI:10.1016/j.jphotochem.2024.115863
日期:——
The acidic ionic liquid [BSO<sub>3</sub>HMIm]HSO<sub>4</sub>: a novel and efficient catalyst for one-pot, three-component syntheses of substituted pyrroles
作者:Yuan Luo、Bao-Qiang Zhang、Yan-Hong He、Zhi Guan
DOI:10.1515/znb-2014-0108
日期:2015.1.1
was used as an efficient catalyst for the synthesis of a variety of pyrrole derivativesvia a one-pot, three-component condensation of amines, nitroolefins, and 1,3-dicarbonylcompounds. Good to excellent yields of 72–96% were obtained under reflux in ethanol. The catalyst could easily be recovered and recycled up to six times, resulting in good yields without prolonging the reaction time. This method