Hydrolysis of 2′-deoxypurine nucleosides. The effect of substitution at the C-8 position
摘要:
The hydrolytic stability of 2'-deoxypurine nucleosides is decreased by introduction of electron-withdrawing substituents at the C-8 position in the series of compounds 2-8, 10-14. The sulfone group causes a 2.9 x 10(4) rate acceleration for glycosidic bond cleavage in compound 14.
Hydrolysis of 2′-deoxypurine nucleosides. The effect of substitution at the C-8 position
摘要:
The hydrolytic stability of 2'-deoxypurine nucleosides is decreased by introduction of electron-withdrawing substituents at the C-8 position in the series of compounds 2-8, 10-14. The sulfone group causes a 2.9 x 10(4) rate acceleration for glycosidic bond cleavage in compound 14.