1058243-77-8Relevant academic research and scientific papers
Synthesis of 3′-deoxy-3′-C-methyl nucleoside derivatives
Aljarah, Mohamed,Couturier, Sarah,Mathé, Christophe,Périgaud, Christian
, p. 7436 - 7442 (2008/12/22)
2′,3′-Dideoxy-3′-C-methyl nucleosides bearing the five naturally occurring nucleic acid bases were synthesized. Additionally, the 3′-deoxy-3′-C-methyl nucleoside analogues bearing 5-aminoimidazole-4-carboxamide as well as 1,2,4-triazole-3-carboxamide moieties were prepared. The synthesis of the corresponding 2′,3′-dideoxy-3′-C-methyl triazole derivative was also accomplished. The dideoxynucleoside derivatives were prepared by radical deoxygenation from their 3′-deoxy-3′-C-methyl parent ribonucleosides. When evaluated for their antiviral activity in cell culture experiments, none of these compounds showed any significant antiviral activity.
Revisited 3′-deoxy-3′-C-methyl-β-D-ribonucleoside series
Aljarah, Mohamed,Couturier, Sarah,Gosselin, Gilles,Mathe, Christophe,Perigaud, Christian
, p. 1125 - 1128 (2008/09/17)
The synthesis of some 3′-deoxy-3′-C-methylnucleoside analogues bearing naturally occuring nucleic acid bases was achieved from the preparation of a suitable peracylated 3-deoxy-3-C-methyl sugar using a stereoselective pathway. In addition, examples of chemical modifications at the 2′ position are presented. Copyright Taylor & Francis Group, LLC.
