Bovine serum albumin catalyzed one-pot, three-component synthesis of dihydropyrano[2,3-c]pyrazole derivatives in aqueous ethanolElectronic supplementary information (ESI) available. CCDC 1432094 and 1432095. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c5ra13014j

Bovine serum albumin (BSA) catalyzed synthesis of dihydropyrano[2,3- c ]pyrazole derivatives via a one pot, three component reaction of an aldehyde/ketone/isatin, malononitrile and 3-methyl-1 H -pyrazol-5-(4 H )-one in H 2 O-EtOH (7 : 3) at ambient temperature was developed in this work. The catalys...

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Main Authors Dalal, Kiran S, Tayade, Yogesh A, Wagh, Yogesh B, Trivedi, Darshak R, Dalal, Dipak S, Chaudhari, Bhushan L
Format Journal Article
Published 04.02.2016
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Summary:Bovine serum albumin (BSA) catalyzed synthesis of dihydropyrano[2,3- c ]pyrazole derivatives via a one pot, three component reaction of an aldehyde/ketone/isatin, malononitrile and 3-methyl-1 H -pyrazol-5-(4 H )-one in H 2 O-EtOH (7 : 3) at ambient temperature was developed in this work. The catalyst was found to work efficiently for aldehydes, ketones and isatins to give the corresponding dihydropyrano[2,3- c ]pyrazole and spiro[indoline-3,4′-pyrano[2,3- c ]pyrazole] derivatives in high yields. BSA showed a broad range of catalytic promiscuity towards various aldehydes, aromatic/aliphatic ketones and substituted isatins. The use of an environmentally benign protocol, reusability of the catalyst, avoidance of hazardous solvents, excellent yields, easy work up and no byproduct formation make BSA an attractive candidate for further applications as a biocatalyst. A BSA catalyzed synthesis of dihydropyrano[2,3- c ]pyrazole derivatives via a one pot, three component reaction of an aldehyde/ketone/isatin, malononitrile and 3-methyl-1 H -pyrazol-5-(4 H )-one in H 2 O-EtOH (7 : 3) at ambient temperature is reported.
Bibliography:Electronic supplementary information (ESI) available. CCDC
For ESI and crystallographic data in CIF or other electronic format see DOI
and
1432095
10.1039/c5ra13014j
1432094
ISSN:2046-2069
DOI:10.1039/c5ra13014j