Synthesis of sialic acid analogues with the oxime group at C-4 or C-5 of KDN

Article abstract of DOI:10.1080/07328309708007331

The readily available methyl (methyl 3-deoxy-5, 8 : 7,9-di-O-isopropylidene-β-D-glycero-D-galacto-2-nonulopyranosid)onate (7) was converted in five synthetic steps into methyl (methyl 4-acetamido-3, 4-dideoxy-β-D-glycero-D-talo-2-nonulopyranosid)onate (11

Full text of DOI:10.1080/07328309708007331

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Journal of Carbohydrate Chemistry
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Synthesis of Sialic Acid Analogues with
the Oxime Group at C-4 Or C-5 of KDN
Toshitsugu Kai a , Xue-Long Sun a , Hiroaki Takayanagi a & Kimio
Furuhata a
a School of Pharmaceutical Sciences, Kitasato University , 5-9-1
Shirokane, Minato-ku, Tokyo, 108, Japan
Published online: 20 Aug 2006.
To cite this article: Toshitsugu Kai , Xue-Long Sun , Hiroaki Takayanagi & Kimio Furuhata (1997)
Synthesis of Sialic Acid Analogues with the Oxime Group at C-4 Or C-5 of KDN , Journal of
Carbohydrate Chemistry, 16:4-5, 521-532, DOI: 10.1080/07328309708007331
To link to this article: http://dx.doi.org/10.1080/07328309708007331
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