-transparent.png){kind=logo}
Several 6-substituted pyrimidine nucleosides have been prepared by condensation of an N(3)-benzyl or C(4)-methylthio pyrimidine with the appropriately blocked sugar, followed by the use of mild conditions at room temperature for removal of blocking groups. The substrate properties of these nucleosides, which are in the fixed syn conformation, have been examined in the uridine phosphorylase system.
Related Publications
K Felczak, and
I Samulewicz, and
A K Drabikowska, and
T Kulikowski, and
D Shugar
October 1974,
Journal of medicinal chemistry,
K Felczak, and
I Samulewicz, and
A K Drabikowska, and
T Kulikowski, and
D Shugar
March 2005,
Chemical & pharmaceutical bulletin,
K Felczak, and
I Samulewicz, and
A K Drabikowska, and
T Kulikowski, and
D Shugar
August 1975,
Annals of the New York Academy of Sciences,
K Felczak, and
I Samulewicz, and
A K Drabikowska, and
T Kulikowski, and
D Shugar
March 1982,
Biochemical pharmacology,
K Felczak, and
I Samulewicz, and
A K Drabikowska, and
T Kulikowski, and
D Shugar
August 1981,
Biochemical pharmacology,
K Felczak, and
I Samulewicz, and
A K Drabikowska, and
T Kulikowski, and
D Shugar
December 1972,
Journal of medicinal chemistry,
K Felczak, and
I Samulewicz, and
A K Drabikowska, and
T Kulikowski, and
D Shugar
April 1996,
Journal of medicinal chemistry,
K Felczak, and
I Samulewicz, and
A K Drabikowska, and
T Kulikowski, and
D Shugar
January 1965,
Chemical & pharmaceutical bulletin,
K Felczak, and
I Samulewicz, and
A K Drabikowska, and
T Kulikowski, and
D Shugar
January 2002,
Nucleosides, nucleotides & nucleic acids,
K Felczak, and
I Samulewicz, and
A K Drabikowska, and
T Kulikowski, and
D Shugar
June 1991,
Biochemical pharmacology,
