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Functionalization of a cis-diol system of ribonucleosides using anhydrocyclic structures
Subtitle:Functionalization of a cis-diol system of ribonucleosides using anhydrocyclic structures
Creator: Publisher:Instytut Chemii Bioorganicznej PAN
Place of publishing: Date issued/created: Description: Degree name: Degree discipline : Type of object: Abstract:Nucleosides modified in the 2’ and 3’ positions are known for many years and involve many important, bioactive compounds. This group consist of derivatives of 2’,3’-dideoxy or 2’,3’-dideoxy-didehydro types, derivatives with additional substituents or substituents instead of hydroxyl groups. These compounds are targeted against viruses and tumors. Anhydrocyclic structures have been known since the middle of the 20th century. However, their utility seems not to be fully explored and described. The number of possible to obtain through anhydrocyclic synthons 2’,3’-dimodified derivatives is very vast, taking under consideration different combinations of S-alkyl, S-aryl, O-alkyl, O-aryl, halogen, triazole, amine and azide substituents in both pyrimidine and purine nucleosides.
Start page: End page: Resource type: Detailed Resource Type: Format: Resource Identifier: Language: Language of abstract: Rights:Creative Commons Attribution BY-SA 4.0 license
Terms of use: Digitizing institution:Institute of Bioorganic Chemistry of the Polish Academy of Science
Original in:Institute of Bioorganic Chemistry of the Polish Academy of Science
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