AbstractAn efficient, convenient method for the synthesis of 3,4-dihydropyrano[3,2-c]chromene derivatives by one-pot, three-component reaction of aldehydes, malononitrile/cyanoacetate, and 4-hydroxycoumarin in the presence of a catalytic amount of thiourea dioxide, an efficient, reusable organic catalyst, is described. A variety of 3,4-dihydropyrano[3,2-c]chromene derivatives were obtained, and 6-amino-5-cyano-4-phenyl-2-methyl-4H-pyran-3-carboxylic acid ethyl esters were obtained by condensation of aldehydes, malononitrile and ethyl acetoacetate in the presence of thiourea dioxide in aqueous medium. The salient features of the protocol are mild reaction conditions, high yields, short reaction time, safety, high atom-economy, eco-friendly s...
A green and operationally simple approach domino reaction has been developed for the synthesis of 2-...
Background and Aim: In this research, we present a three-component method for the preparation of 3,4...
<p>An efficient and eco-friendly procedure for the synthesis of 2-amino-5-oxo-4-aryl-4<i>H</i>,5<i>H...
AbstractAn efficient, convenient method for the synthesis of 3,4-dihydropyrano[3,2-c]chromene deriva...
We report ammonium metavanadate catalyzed one-pot synthesis of 3,4-dihydropyrano[3,2-c]chromenes, fr...
An efficient and convenient method has been developed for the synthesis of 2- amino-5-oxo-4-phenyl-4...
This article presents a simple and practical method for the synthesis of 3,4-dihydropyrano[c]chromen...
Research Department of Chemistry, Bioactive Organic Molecule Synthetic Unit, C. Abdul Hakeem College...
ABSTRACT. Highly efficient, three-component condensation of aromatic aldehyde, malononitrile and 4-h...
Ultrasound promoted mild one-pot multicomponent synthesis of 3,4-dihydropyrano[c]chromenes from 4-hy...
An easy solvent-free method is described for the synthesis of 3,4-dihydropyrano[c]chromenes by a one...
Disodium phosphate catalyzed one-pot synthesis of 3,4-dihydropyrano[3,2-c]chromenes, from alde...
Dihydropyrano[3,2-b]chromenedione derivatives were synthesized in moderate-to-high yields in one-pot...
Published ArticleOne-pot efficient protocol to the synthesis of 2-amino-5-oxo-4,5-dihydropyrano(3,2-...
A simple, efficient, solventless, and one step, B(C6F5)3 catalyzed, synthesis of dihydropyrano[3,2-b...
A green and operationally simple approach domino reaction has been developed for the synthesis of 2-...
Background and Aim: In this research, we present a three-component method for the preparation of 3,4...
<p>An efficient and eco-friendly procedure for the synthesis of 2-amino-5-oxo-4-aryl-4<i>H</i>,5<i>H...
AbstractAn efficient, convenient method for the synthesis of 3,4-dihydropyrano[3,2-c]chromene deriva...
We report ammonium metavanadate catalyzed one-pot synthesis of 3,4-dihydropyrano[3,2-c]chromenes, fr...
An efficient and convenient method has been developed for the synthesis of 2- amino-5-oxo-4-phenyl-4...
This article presents a simple and practical method for the synthesis of 3,4-dihydropyrano[c]chromen...
Research Department of Chemistry, Bioactive Organic Molecule Synthetic Unit, C. Abdul Hakeem College...
ABSTRACT. Highly efficient, three-component condensation of aromatic aldehyde, malononitrile and 4-h...
Ultrasound promoted mild one-pot multicomponent synthesis of 3,4-dihydropyrano[c]chromenes from 4-hy...
An easy solvent-free method is described for the synthesis of 3,4-dihydropyrano[c]chromenes by a one...
Disodium phosphate catalyzed one-pot synthesis of 3,4-dihydropyrano[3,2-c]chromenes, from alde...
Dihydropyrano[3,2-b]chromenedione derivatives were synthesized in moderate-to-high yields in one-pot...
Published ArticleOne-pot efficient protocol to the synthesis of 2-amino-5-oxo-4,5-dihydropyrano(3,2-...
A simple, efficient, solventless, and one step, B(C6F5)3 catalyzed, synthesis of dihydropyrano[3,2-b...
A green and operationally simple approach domino reaction has been developed for the synthesis of 2-...
Background and Aim: In this research, we present a three-component method for the preparation of 3,4...
<p>An efficient and eco-friendly procedure for the synthesis of 2-amino-5-oxo-4-aryl-4<i>H</i>,5<i>H...