ePrints@IIScePrints@IISc Home | About | Browse | Latest Additions | Advanced Search | Contact | Help

A norbornyl route to cyclohexitols: structural diversity in fragmentation through functional group switching. Synthesis of alpha- and beta-galactose, alpha-talose and alpha-fucopyranose carbasugars

Mehta, Goverdhan and Mohal, Narinder and Lakshminath, Sripada (2000) A norbornyl route to cyclohexitols: structural diversity in fragmentation through functional group switching. Synthesis of alpha- and beta-galactose, alpha-talose and alpha-fucopyranose carbasugars. In: Tetrahedron Letters, 41 (18). pp. 3505-3508.

[img]
Preview
PDF
Fucopyranose_carbasugars.pdf

Download (253Kb)

Abstract

A novel fragmentation sequence has been executed within the norbornane system, involving C1–C7 bond scission, to extract a versatile, highly functionalized cyclohexanoid moiety. Its further evolution towards a range of carbasugars is described.

Item Type: Journal Article
Additional Information: Copyright for this article belongs to Elsevier Science.
Keywords: Fragmentation reactions;Carbasugars;Hydroxylation
Department/Centre: Division of Chemical Sciences > Organic Chemistry
Date Deposited: 12 Aug 2004
Last Modified: 19 Sep 2010 04:14
URI: http://eprints.iisc.ernet.in/id/eprint/1263

Actions (login required)

View Item View Item