Synthesis and reactions of 3-C-branched-chain analogues of 3,6-anhydrodeoxynojirimycin

Article abstract of DOI:10.1080/07328309708006509

The syntheses of 3,6-anhydro-1-deoxy-3-C-ethoxycarbonylmethyl- (4) and 3-C-(2-hydroxyethyl)nojirimycin (5) from 5-azido-6-O-tert-butyldiphenylsilyl-5-deoxy-1,2-O-isopropylidene-α-D- glucofuranose (8) are described. The key intermediate is 5-azido-6-O-tert

Full text of DOI:10.1080/07328309708006509

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Journal of Carbohydrate Chemistry
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Synthesis and Reactions of 3-C-
Branched-Chain Analogues of 3,6-
Anhydrodeoxynojirimycin
C. Kuan Lee a , Huixin Jiang a & A. M. Scofield b
a Department of Chemistry , National University of Singapore , Kent
Ridge, 0511
b Department of Biochemistry and Biological Sciences , University of
London , Wye College, Wye, Ashford, Kent, TN25 5AH, UK
Published online: 21 Aug 2006.
To cite this article: C. Kuan Lee , Huixin Jiang & A. M. Scofield (1997) Synthesis and Reactions of 3-C-
Branched-Chain Analogues of 3,6-Anhydrodeoxynojirimycin , Journal of Carbohydrate Chemistry, 16:1,
49-62
To link to this article: http://dx.doi.org/10.1080/07328309708006509
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