Efficient Electrochemical <i>N</i>-Glycosylation of Silylated Pyrimidines with Protected Arylthioriboses in the Presence of a Catalytic Amount of NBS or Br2
Junzo NokamiDepartment of Applied Chemistry, Faculty of Engineering, Okayama University of ScienceRidai-cho, OkayamaMasahiro OsafuneDepartment of Applied Chemistry, Faculty of Engineering, Okayama University of ScienceRidai-cho, OkayamaY. ITODepartment of Applied Chemistry, Faculty of Engineering, Okayama University of ScienceRidai-cho, OkayamaF MiyakeDepartment of Applied Chemistry, Faculty of Engineering, Okayama University of ScienceRidai-cho, OkayamaShin‐ichi SumidaDepartment of Applied Chemistry, Faculty of Engineering, Okayama University of ScienceRidai-cho, OkayamaSigeru Torii
1999en
ABI
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Abstract Electrolysis of silylated pyrimidines with protected arylthioribose, in the presence of a catalytic amount of NBS or Br2 as a mediator in an undivided cell, gave the corresponding N-glycosides (nucleosides) in good yield.
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