New methodologies for the synthesis of C-2 functionalized hypoxanthine nucleosides
- 1 June 1988
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 53 (13) , 3051-3057
- https://doi.org/10.1021/jo00248a027
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Synthesis and anti-HIV activity of various 2'- and 3'-substituted 2',3'-dideoxyadenosines: a structure-activity analysisJournal of Medicinal Chemistry, 1987
- Long-term inhibition of human T-lymphotropic virus type III/lymphadenopathy-associated virus (human immunodeficiency virus) DNA synthesis and RNA expression in T cells protected by 2',3'-dideoxynucleosides in vitro.Proceedings of the National Academy of Sciences, 1987
- Novel photoinduced functionalized C-alkylations in purine systemsThe Journal of Organic Chemistry, 1985
- Substrate specificity of adenosine deaminase—Function of the 5′-hydroxyl group of adenosineBioorganic Chemistry, 1980
- Utility of purinyl radicals in the synthesis of base-modified nucleosides and alkylpurines: 6-amino group replacement by hydrogen, chlorine, bromine, and iodineThe Journal of Organic Chemistry, 1980
- The synthesis of oligoribonucleotides. II. The use of silyl protecting groups in nucleoside and nucleotide chemistry. VIICanadian Journal of Chemistry, 1978
- The Role of the 5′-Hydroxyl Group of Adenosine in Determining Substrate Specificity for Adenosine DeaminaseJournal of Medicinal Chemistry, 1967