EFFICIENT SOLID-PHASE SYNTHESIS OF ISOCYTOSINE DERIVATIVES
DOI:
https://doi.org/10.1007/6449Keywords:
isocytosines, "addition-elimination" mechanism, antiviral activity, solid-phase synthesisAbstract
We have investigated the potential use of a solid-phase synthesis of novel 6-(arylmethyl)-5-methyl-isocytosine derivatives based on the immobilization of the corresponding 2-thiothymine on a Merrifield
resin, oxidation of the immobilized form to the sulfone, and aminolysis of the latter under mild conditions.
How to Cite
Novakov, I. A.; Orlinson, B. S.; Brunilin, R. V.; Nawrozkij, M. B.; Gordeeva, E. A.; Savel'ev, E. N.; Gerasimov, E. N. Chem. Heterocycl. Compd. 2009, 45, 1365. [Khim. Geterotsikl. Soedin. 2009, 1697.]
For this article in the English edition see DOI10.1007/s10593-010-0434-0