Journal
LETTERS IN ORGANIC CHEMISTRY
Volume 10, Issue 4, Pages 245-251Publisher
BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/1570178611310040004
Keywords
ZnS-nanoparticles; chalcones; azomethine ylide; multicomponent reaction; spiro-heterocycles
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ZnS-nanoparticles, as recyclable heterogeneous catalyst, efficiently promoted in the synthesis of spiro[pyrrolidine-2,3'-oxindole] derivatives through three-component reaction of isatin, alpha-amino acid and phenothiazinyl chalcones. An azomethine ylide generated by decarboxylative condensation of isatin with alpha-amino acid, and chalcones have been used as trapping dipolarophiles. ZnS nanoparticles were synthesized by aqueous chemical method. The advantages of this method lie in its simplicity, cost effectiveness, and easier scaling up for large scale synthesis.
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