Synthesis of (+/−)–1′-Aza-carbocyclic-pyrimidine-2′,3′-dideoxynucleoside analogues as potential anti-HIV agents
- 1 January 1991
- journal article
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 1 (12) , 757-760
- https://doi.org/10.1016/s0960-894x(01)81063-5
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Synthesis of pyrrolidin-1-yl analogues of pyrimidine dideoxynucleosidesTetrahedron Letters, 1991
- Synthesis of ()-2′-oxa-carbocyclic-2′,3′-dideoxynucleosides as potential anti-HIV agentsTetrahedron Letters, 1991
- Tetrahydrothiophene nucleosides as potential anti-HIV agentsTetrahedron Letters, 1991
- A ring-enlarged oxetanocin A analog as an inhibitor HIV infectivityJournal of Medicinal Chemistry, 1991
- Synthesis of novel 1′-nitrogen replaced carbocyclic thymidine analogs as potential anti aids agentsBioorganic & Medicinal Chemistry Letters, 1991
- Molecular Targets for AIDS TherapyScience, 1990
- Synthesis and anti-HIV activity of carbocyclic 2',3'-didehydro-2',3'-dideoxy 2,6-disubstituted purine nucleosidesJournal of Medicinal Chemistry, 1990
- (±)-Dioxolane-T ((±)-1-[(2β,4β)-2-(hydroxymethyl)-4-dioxolanyl]thymine): A new 2′,3′-dideoxynucleoside prototype within vitro activity against HIVTetrahedron Letters, 1989
- Synthesis of iso-ddA, member of a novel class of anti-HIV agentsTetrahedron Letters, 1989
- Reduction of nitrosamines with aqueous titanium trichloride: convenient preparation of aliphatic hydrazinesThe Journal of Organic Chemistry, 1984