Organic chemistry
Zahra Vafajoo; Davood Kordestani; Saba Vafajoo
Volume 6, Issue 3, pp. 218-324, Serial No. 20 , July 2018, , Pages 293-299
Abstract
2-Amino-5,10-dioxo-4-aryl-5,10-dihydro-4H-benzo[g]chromene-3-carbonitrile derivatives are obtained in excellent yields with a simple and efficient procedure.This reaction can occur using electrocatalytic multicomponent chain transformation of aryl aldehydes, 2-hydroxynaphthalene-1,4-dione and malononitrile ...
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2-Amino-5,10-dioxo-4-aryl-5,10-dihydro-4H-benzo[g]chromene-3-carbonitrile derivatives are obtained in excellent yields with a simple and efficient procedure.This reaction can occur using electrocatalytic multicomponent chain transformation of aryl aldehydes, 2-hydroxynaphthalene-1,4-dione and malononitrile under neutral and mild conditions. Moreover, electrolysis is done in CH3CN as solvent, Tetrabutylammonium fluoride (TBAF) as an effective supporting electrolyte and an iron electrode as the cathode and a graphite electrode as the anode in undivided cell. Also Excellent conversions of the starting materials were obtained under 10 mA/cm2 current densities after 0.54 F/mol of electricity had been passed and I=50 mA at room temperature. The key advantages of this method are the high yields, simple work up the non-chromatographic purification of products.
Organic chemistry
Hemant Chavan; Datta Survase; Sakharam Dongare; Vasant Helavi; Shreeram Ganapure
Volume 5, Issue 1, pp. 1-120, Serial No. 14 , January 2017, , Pages 105-114
Abstract
Regioselective synthesis of highly functionalized pyranopyrazoles was achieved in excellent yield from phenyl pyrazolone, substituted aromatic aldehyde with nitroketene-N,S-acetal in the presence of indium trichloride as a versatile catalyst under reflux condition in ethanol-water mixture. All reactions ...
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Regioselective synthesis of highly functionalized pyranopyrazoles was achieved in excellent yield from phenyl pyrazolone, substituted aromatic aldehyde with nitroketene-N,S-acetal in the presence of indium trichloride as a versatile catalyst under reflux condition in ethanol-water mixture. All reactions preceeded within a short period of time with excellent purity. All of the synthesized compounds were identified by IR, 1H NMR, 13C NMR and mass spectroscopy. Quantitative yields, inexpensive and environmentally friendly solvent system and simple work-up procedure are the attractive features of the present method. It is thus enviro-economic method without producing hazardous wastes. The formed pyranopyrazoles might find to possess important biological and pharmaceutical applications.