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Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/308

Title: Diastereoselective synthesis of glycosylated prolines as α-glucosidase inhibitors and organocatalyst in asymmetric aldol reaction
Authors: Pandey, Jyoti
Dwivedi, Namrata
Srivastava, A K
Tamarkar, A
Tripathi, R P
Issue Date: 2007
Citation: Bioorganic & Med. Chem. Letters 17, 1321 (2007)
Series/Report no.: CDRI Communication No 7057
Abstract: 1,3-Dipolar cycloaddition of azomethine ylides and glycosyl E-olefins in presence of LDA led to diastereoselective formation of C-glycosylated proline esters. The selected esters on regioselective hydrolysis with LiOH gave C-glycosyl prolines. Few of the proline esters exhibited very good α-glucosidase inhibitory activity. The organocatalytic activity of one of the prolines in a prototype Aldol reaction has also been established.
URI: http://hdl.handle.net/123456789/308
Appears in Collections:Medicinal and Process Chemistry

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