A norbornyl route to cyclohexitols: structural diversity in fragmentation through functional group switching. synthesis of α- and β-galactose, α-talose and α-fucopyranose carbasugars

Mehta, Goverdhan ; Mohal, Narinder ; Lakshminath, Sripada (2000) A norbornyl route to cyclohexitols: structural diversity in fragmentation through functional group switching. synthesis of α- and β-galactose, α-talose and α-fucopyranose carbasugars Tetrahedron Letters, 41 (18). pp. 3505-3508. ISSN 0040-4039

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Official URL: http://linkinghub.elsevier.com/retrieve/pii/S00404...

Related URL: http://dx.doi.org/10.1016/S0040-4039(00)00408-1

Abstract

A novel fragmentation sequence has been executed within the norbornane system, involving C₁-C₇bond scission, to extract a versatile, highly functionalized cyclohexanoid moiety. Its further evolution towards a range of carbasugars is described.

Item Type:	Article
Source:	Copyright of this article belongs to Elsevier Science.
Keywords:	Fragmentation Reactions; Carbasugars; Hydroxylation
ID Code:	28950
Deposited On:	18 Dec 2010 05:46
Last Modified:	17 May 2016 11:57

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