In this paper, an environmentally benign, convenient, and efficient one-pot three-component
reaction has been developed for the regioselective synthesis of novel 5-aroyl (or …

A series of N‐arylpyrimido [4, 5‐b] quinolines 3a–e and 2‐aryl‐2, 3‐dihydropyrimido [4, 5‐b]
quinoline‐4 (1 H)‐ones 5a–e was designed and synthesized as potential anticancer agents …

A series of novel N‐aryl‐5‐aryl‐6, 7, 8, 9‐tetrahydropyrimido [4, 5‐b] quinolin‐4‐amines 4a–
4l was synthesized as potential anticancer agents through Dimroth rearrangement reaction …

To tackle the environmental unfriendly issue in existing synthesis strategies for 6-substitued
thiopurine derivatives, such as poor step economy, frequent use of malodorous organic …

New complexes I–IV of di-tert-butyltin with ligands based on heterocyclic thioamides (2-
mercaptobenzoxazole, 2-mercaptobenzothiazole, 2-mercaptobenzimidazole) and 2, 6-di-tert …

We introduce the synthesis and characterization of a novel purine derivative, 2-amino-6‑
chloro-N, N-diphenyl-7H-purine-7-carboxamide. X-ray crystallography was utilized to …

Cancer is still the leading cause of death in both developing and economically developed
countries. There is still a need to create new drugs with higher efficacy despite substantial …

The reaction of 5-(4-methoxyphenyl) furan-2, 3-dione with urea in a 1: 1 ratio when refluxed
in a mixture of 1, 2-dichloroethane-DMSO gives (Z)-N-carbamoyl-4-hydroxy-4-(4 …