Oxidation products of C-4 and C-7 hydroxyls in the methyl α-glycoside derivatives of KDN

Article abstract of DOI:10.1080/07328309708007332

A regioselective protection of hydroxyl groups in the methyl ester-methyl α-glycoside derivative of KDN was demonstrated. Isopropylidenation of methyl (methyl 3-deoxy-α-D-glycero-D-galacto-2-nonulopyranosid)onate (1) gave mono-(8, 9) and di-(5, 7: 8, 9) O

Full text of DOI:10.1080/07328309708007332

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Journal of Carbohydrate Chemistry
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Oxidation Products of C-4 and C-7
Hydroxyls in the Methyl α-Glycoside
Derivatives 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)
Oxidation Products of C-4 and C-7 Hydroxyls in the Methyl α-Glycoside Derivatives of KDN , Journal of
Carbohydrate Chemistry, 16:4-5, 533-540, DOI: 10.1080/07328309708007332
To link to this article: http://dx.doi.org/10.1080/07328309708007332
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