62374-32-7Relevant articles and documents
The synthesis and biological evaluation of nucleobases/tetrazole hybrid compounds: A new class of phosphodiesterase type 3 (PDE3) inhibitors
Shekouhy, Mohsen,Karimian, Somaye,Moaddeli, Ali,Faghih, Zeinab,Delshad, Yousef,Khalafi-Nezhad, Ali
, (2020/05/18)
Spired by the chemical structure of Cilostazol, a selective phosphodiesterase 3A (PDE3A) inhibitor, several novel hybrid compounds of nucleobases (uracil, 6-azauracil, 2-thiuracil, adenine, guanine, theophylline and theobromine) and tetrazole were designe
Silica sulfuric acid (SSA) as a highly efficient heterogeneous catalyst for persilylation of purine and pyrimidine nucleobases and other N-heterocycles using HMDS
Rad, Mohammad Navid Soltani,Khalafi-Nezhad, Ali,Divar, Masoumeh,Behrouz, Somayeh
experimental part, p. 1943 - 1954 (2010/11/16)
Purine and pyrimidine nucleobases and other N-heterocycles have been silylated with HMDS in excellent yields in the presence of a catalytic amount of silica sulfuric acid (SSA) as a heterogeneous catalyst. SSA utilizes a shorter reaction time and higher yields of silylated nucleobases. SSA is reusable for several times without a decrease in reactivity or yield of silylated adducts. Copyright
Synthesis of 8-substituted theophylline β-D-ribofuranosides
Ozola,Ramzaeva,Maurinsh,Lidaks
, p. 827 - 839 (2007/10/02)
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