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.

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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
Publication:	Tetrahedron Letters
Publisher:	Elsevier Science
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.ac.in/id/eprint/1263

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