Stereocontrolled preparation of cyclic xanthate; a novel synthetic route to 4-thiofuranose and 4′-thionucleoside
- 1 January 1991
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Chemical Communications
- No. 20,p. 1421-1422
- https://doi.org/10.1039/c39910001421
Abstract
Optically active cyclic xanthate was prepared by the reaction of an epoxy alcohol with NaH and CS2, and was found to be a useful intermediate for synthesis of 4-thio-2-deoxyribose and 4′-thio-2′-deoxyribonucleoside.Keywords
This publication has 13 references indexed in Scilit:
- Synthesis of ()-2′-oxa-carbocyclic-2′,3′-dideoxynucleosides as potential anti-HIV agentsTetrahedron Letters, 1991
- Tetrahydrothiophene nucleosides as potential anti-HIV agentsTetrahedron Letters, 1991
- Synthesis and anti-HIV activity of carbocyclic 2',3'-didehydro-2',3'-dideoxy 2,6-disubstituted purine nucleosidesJournal of Medicinal Chemistry, 1990
- Synthesis of iso-ddA, member of a novel class of anti-HIV agentsTetrahedron Letters, 1989
- Asymmetric Epoxidation of Allylic Alcohols: The Sharpless EpoxidationSynthesis, 1986
- Titanium isopropoxide-mediated nucleophilic openings of 2,3-epoxy alcohols. A mild procedure for regioselective ring-openingThe Journal of Organic Chemistry, 1985
- Total synthesis of carbohydrates: stereoselective syntheses of 2,6-dideoxy-D-arabino-hexose and 2,6-dideoxy-D-ribo-hexoseThe Journal of Organic Chemistry, 1982
- Stereocontrolled synthesis of D-pentitols, 2-amino-2-deoxy-D-pentitols and 2-deoxy-D-pentitols from D-glyceraldehyde acetonideJournal of the American Chemical Society, 1982
- Kinetic resolution of racemic allylic alcohols by enantioselective epoxidation. A route to substances of absolute enantiomeric purity?Journal of the American Chemical Society, 1981
- The first practical method for asymmetric epoxidationJournal of the American Chemical Society, 1980