Journal of Capital Medical University ›› 2012, Vol. 33 ›› Issue (5): 653-655.doi: 10.3969/j.issn.1006-7795.2012.05.020

• 基础研究 • Previous Articles     Next Articles

Investigation on the synthetic reaction of glucopyranosides

ZHANG Jian-wei, FAN Yuan-jie   

  1. Department of Chemistry and Biochemistry, College of Pharmaceutical Sciences, Capital Medical University, Beijing 100069, China
  • Received:2012-05-14 Revised:1900-01-01 Online:2012-10-21 Published:2012-10-21

Abstract: Objective To investigate synthesis of thymine nucleoside.Methods The reactions of phenyl 3,4,6-Tri-O-acetyl-2-deoxy-2-phthalimido-1-thio-β-glucopyranoside and phenyl 3,4-Di-O-benzoyl-6-O-acetyl-2-deoxy-2-phthalimido-1-thio-β-glucopyranoside with the silylated thymine were allowed to occur in dichlormethane. Results The 3,4,6-Tri-O-acetyl-2-deoxy-2-phthalimido-1-thio-β-glucopyranosideand phenyl 3,4-Di-O-benzoyl-6-O-acetyl-2-deoxy-2-phthalimido-1-thio-glucopyranoside reacted with the silylated thymine to form N-β-glycoside. Conclusion Thus we have explored the reaction glucopyranosides with thymine. phenyl 3,4,6-Tri-O-acetyl-2-deoxy-2-phthalimido-1-thio-β-glucopyranoside and phenyl 3,4-Di-O-benzoyl-6-O-acetyl-2-deoxy-2-phthalimido-1-thio-β-glucopyranoside furnished N1-β-glycosideand N3-β-glycoside.

Key words: glucosamine, thymine, nucleoside

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