Recent studies from this laboratory have shown that 6,5'-cyclopyrlmidine nucleosides2, for example the isopropylideneuridine analogue 1, are very susceptible to oxidation at C-5'. Thus, autoxidation3 of 1. with 02-NaOH, or treatment with Mn02 in methanol readily affords the 5'-ketonucleoside 4. The
โฆ LIBER โฆ
A new class of pyrimidine nucleosides: inhibitors of hepatitis B and C viruses
โ Scribed by Shakya, Neeraj; Vedi, Satish; Liang, Chao; Agrawal, Babita; Lorne Tyrrell, D.; Kumar, Rakesh
- Book ID
- 122072124
- Publisher
- Elsevier Science
- Year
- 2012
- Tongue
- English
- Weight
- 537 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0960-894X
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
Nucleosides CXI. 6,6โฒ-Anhydro-hexofurano
โ
Brian A. Otter; Elvira A. Falco
๐
Article
๐
1978
๐
Elsevier Science
๐
French
โ 269 KB
Synthesis of 2-(ฮฒ-D-ribofuranosyl)pyrimi
โ
Timothy A. Riley; William J. Hennen; N. Kent Dalley; Bruce E. Wilson; Roland K.
๐
Article
๐
1987
๐
Journal of Heterocyclic Chemistry
๐
English
โ 766 KB
Synthesis of hemslecin A derivatives: A
โ
Guo, Rui-Hua; Geng, Chang-An; Huang, Xiao-Yan; Ma, Yun-Bao; Zhang, Quan; Wang, L
๐
Article
๐
2013
๐
Elsevier Science
๐
English
โ 460 KB
ChemInform Abstract: Aza-C-nucleosides a
โ
Mads D. Soerensen; Nagy M. Khalifa; Erik B. Pedersen
๐
Article
๐
2010
๐
John Wiley and Sons
โ 26 KB
๐ 2 views
Nucleosides XCIII. Synthesis of 6-ฮฒ-d-ri
โ
Steve Y-K. Tam; Federico G. De Las Heras; Robert S. Klein; Jack J. Fox
๐
Article
๐
1975
๐
Elsevier Science
๐
French
โ 220 KB
Recent reports have dealt with the preparation of functionalized C-glycosyl compounds 2 as synthetic intermediates for the preparation of naturally occurring C-nucleosides and their analogues 2a\*d-g. As part of our general program on the synthesis of C-nucleosides, we have prepared the new C-glycos
Design and Synthesis of Novel 5-Substitu
โ
Kumar, Rakesh; Nath, Mahendra; Tyrrell, D. Lorne J.
๐
Article
๐
2002
๐
American Chemical Society
๐
English
โ 107 KB