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Stereoselective syntheses of aminocyclopentitols: a norbornyl approach

Mehta, Goverdhan and Mohal, Narinder (2001) Stereoselective syntheses of aminocyclopentitols: a norbornyl approach. In: Tetrahedron Letters, 42 (25). pp. 4227-4230.


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Synthesis of some novel aminocyclopentitol analogues has been achieved through a functionally embellished cyclopentanoid derivative of well-defined stereochemical disposition, obtained via a Grob-type fragmentation sequence executed within the norbornyl framework. The glycosidase inhibition studies of the new aminocyclopentitols indicate them to be weak inhibitors.

Item Type: Journal Article
Publication: Tetrahedron Letters
Publisher: Elsevier Science
Additional Information: Copyright for this article belongs to Elsevier Science.
Keywords: aminocyclopentitol;glycosidase inhibitor;carbocyclic nucleosides
Department/Centre: Division of Chemical Sciences > Organic Chemistry
Date Deposited: 31 Jan 2005
Last Modified: 19 Sep 2010 04:17
URI: http://eprints.iisc.ac.in/id/eprint/2685

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