Some new spiro[oxindole-quinazoline/pyrimidine]ones were synthesized via a novel three-component Biginelli-like reaction between isatin, cyclic or acyclic 1,3-dicarbonylcompounds, and urea, N-methyl urea or thiourea in one pot and good yields.
A novel one-pot synthesis of spirooxindole derivatives catalyzed by nano ZnO
作者:B. Baghernejad、M. Khorshidi
DOI:10.4314/bcse.v27i2.17
日期:——
Nano zinc oxide was explored as a heterogeneous and reusable catalyst for the one-pot synthesis of spirooxindoles via three-component reaction between urea, isatin, and 1,3-dicarbonyl compounds.
Novel One-Pot Synthesis of New Oxindole Derivatives Catalyzed by PTSA
作者:Maliheh Khorshidi、Majid M. Heravi、Yahia S. Beheshtia、Bita Baghernejad
DOI:10.1080/00397911.2010.515364
日期:2011.10
Abstract The one-pot synthesis of spirooxindoles via three-component reaction of urea, isatin, and 1,3-dicarbonyl compounds in the presence of a catalytic amount of p-toluenesulfonic acid in acetonitrile has been carried out.
Novel spiro-oxindole derivatives were synthesised by one-pot multicomponent reaction using isatins, urea and 1,3-dicarbonyls. -Cyclodextrin, an oligosaccharide, catalysed the reaction and can be reused for further reaction after recovery. This developed synthetic route is environmentally benign in which water is used as solvent to produce excellent yields of products. The synthesised compounds were evaluated for their antimicrobial activities against two bacteria and two fungi. All the synthesised spiro-oxindoles exhibit significant antimicrobial activity.