Synthesis and chemistry of some pyridazine nucleosides related to certain 5-substituted pyrimidine nucleosides
نویسندگان
چکیده
منابع مشابه
Cytidine nucleosides II. Photochemical synthesis of 5-alkylcytidine nucleosides
5-Alkylcytidine nucleosides were synthesized via a photocoupling reaction. 5-Propylcytidine and 5-propyl-2-deoxycytidine have been prepared through the reduction of 5-(3-propenyl)cytidine and its 2'-deoxy derivative, which in turn were prepared by photoirradiation of cytidine or 2'-deoxycytidine in the presence of 3-iodopropene. 5-(2-Hydroxyethyl)cytidine and its derivatives were obtained from ...
متن کاملSynthesis and solvatochromic fluorescence of biaryl pyrimidine nucleosides.
Fluorescent pyrimidine analogs containing a fused biphenyl unit were prepared in high yields using stereoselective N-glycosylation and Suzuki-Miyaura cross-coupling reactions. The resulting "push-pull" fluorophores exhibit highly solvatochromic emissions from twisted intramolecular charge-transfer (TICT) states.
متن کاملMetabolism of pyrimidine L-nucleosides.
The intraperitoneal application of L-nucleosides (L-Cyd, L-Urd, L-dThd) to mice results in distribution of these compounds into tissues of the organism and their gradual excretion in the unchanged form. The residual level has been observed with L-ribonucleosides only and contains in addition to the L-nucleoside its 5'-phosphate. The phosphorylation in vivo is catalyzed by nucleoside-kinase and ...
متن کاملA general approach to the synthesis of 5-S-functionalized pyrimidine nucleosides and their analogues.
A general and efficient approach was developed for the introduction of S-functionality at the C-5 position of cytosine and uracil nucleosides and their analogues. The key step is a palladium-catalyzed C-S coupling of the corresponding 5-bromo nucleoside derivative and alkyl thiol. The butyl 3-mercaptopropionate coupling products were further converted to the corresponding disulphides, the stabl...
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ژورنال
عنوان ژورنال: Journal of Heterocyclic Chemistry
سال: 1983
ISSN: 0022-152X,1943-5193
DOI: 10.1002/jhet.5570200221