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

Authors
Mehta, G Mohal, N Lakshminath, S
Citation
G. Mehta et al., 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, TETRAHEDR L, 41(18), 2000, pp. 3505-3508
Citations number
25
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON LETTERS
ISSN journal
00404039 → ACNP
Volume
41
Issue
18
Year of publication
2000
Pages
3505 - 3508
Database
ISI
SICI code
0040-4039(20000429)41:18<3505:ANRTCS>2.0.ZU;2-A
Abstract
A novel fragmentation sequence has been executed within the norbornane syst em, involving C-1-C-7 bond scission, to extract a versatile, highly functio nalized cyclohexanoid moiety. Its further evolution towards a range of carb asugars is described. (C) 2000 Elsevier Science Ltd. All rights reserved.