β-Selective synthesis of 2'-deoxynucleosides by the coupling of 2-deoxy-1-thio-D-threo-pentofuranosides with silylated thymine
- 28 April 1992
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 33 (18) , 2515-2516
- https://doi.org/10.1016/s0040-4039(00)92229-9
Abstract
No abstract availableThis publication has 16 references indexed in Scilit:
- A general method for controlling glycosylation stereochemistry in the synthesis of 2′-deoxyribose nucleosidesTetrahedron Letters, 1990
- Stereoselectivity in the Coupling Reaction between 2-Phenylthio-2,3-dideoxyribose and Silylated Pyrimidine BasesChemistry Letters, 1990
- Targets and strategies for the antiviral chemotherapy of AIDSTrends in Pharmacological Sciences, 1990
- Chapter 16. Recent Advances in Anti-retroviral Chemotherapy for AIDSPublished by Elsevier ,1990
- New acquisitions in the development of anti-HIV agentsAntiviral Research, 1989
- Stereoselective Synthesis of β-2-Deoxyribonucleosides from 1-O-Acetyl-3-O-[2-(methylsulfinyl)ethyl]-2-deoxyriboseChemistry Letters, 1989
- The Synthesis of 2′-Deoxyadenosine via Stereospecific Coupling ReactionChemistry Letters, 1989
- Chapter 14. Antiviral AgentsPublished by Elsevier ,1989
- Stereoselective Synthesis of Anomers of 5-Substituted 2′-DeoxyuridinesBulletin of the Chemical Society of Japan, 1987
- Stereochemical control as a function of protecting-group participation in 2-deoxy-D-erythro-pentofuranosyl nucleosidesCarbohydrate Research, 1981