78138-03-1Relevant articles and documents
Efficient electrochemical N-glycosylation of silylated pyrimidines with protected arylthioriboses in the presence of a catalytic amount of NBS or Br2
Nokami, Junzo,Osafune, Masahiro,Ito, Yuichiro,Miyake, Fumiaki,Sumida, Shin-Ichi,Torii, Sigeru
, p. 1053 - 1054 (1999)
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.
STEREOCHEMICAL CONTROL AS A FUNCTION OF PROTECTING-GROUP PARTICIPATION IN 2-DEOXY-D-ERYTHRO-PENTOFURANOSYL NUCLEOSIDES
Wierenga, Wendell,Skulnick, Harvey I.
, p. 41 - 52 (2007/10/02)
Possible features controlling the anomeric ratios in the synthesis of the antiviral antibiotic dihydro-5-azathymidine have been examined.Replacement of the 3- and 5-(4-methylbenzoyl) protecting groups in 2-deoxy-D-erythro-pentofuranosyl chloride by benzyl