Selenium-controlled stereoselective synthesis of 2′-deoxynucleosides from glycals. A formal synthesis of AZT
- 1 April 1993
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 34 (17) , 2821-2822
- https://doi.org/10.1016/s0040-4039(00)73571-4
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Facile, highly stereoselective synthesis of 2′,3′-dideoxy- and 2′,3′-didehydro-2′,3t'-dideoxy nucleosides via a furanoid glycal intermediateTetrahedron Letters, 1992
- A highly stereoselective synthesis of anti-HIV 2',3'-dideoxy- and 2',3'-didehydro-2',3'-dideoxynucleosidesThe Journal of Organic Chemistry, 1992
- Diastereoselective sulfenylation reactions employing N-phenylthio lactams under nonbasic conditionsThe Journal of Organic Chemistry, 1992
- Selenoxide elimination for the synthesis of unsaturated-sugar uracil nucleosidesThe Journal of Organic Chemistry, 1991
- A general method for controlling glycosylation stereochemistry in the synthesis of 2′-deoxyribose nucleosidesTetrahedron Letters, 1990
- Molecular Targets for AIDS TherapyScience, 1990
- Stereoselectivity in the Coupling Reaction between 2-Phenylthio-2,3-dideoxyribose and Silylated Pyrimidine BasesChemistry Letters, 1990
- Nucleic acid related compounds. 53. Synthesis and biological evaluation of 2′-deoxy-β-threo-pentofuranosyl nucleosides. "Reversion to starting alcohol" in Barton-type reductions of thionocarbonatesCanadian Journal of Chemistry, 1988
- 3'-Substituted 2',3'-dideoxynucleoside analogs as potential anti-HIV (HTLV-III/LAV) agentsJournal of Medicinal Chemistry, 1987
- Enolate Claisen rearrangement of esters from furanoid and pyranoid glycalsThe Journal of Organic Chemistry, 1980