Synthesis of 3,6-anhydro sugars from cyclic sulfites and sulfates and their applications in the preparation of bicyclonucleoside analogues of ddC andddA

Citation
Mp. Molas et al., Synthesis of 3,6-anhydro sugars from cyclic sulfites and sulfates and their applications in the preparation of bicyclonucleoside analogues of ddC andddA, TETRAHEDRON, 55(51), 1999, pp. 14649-14664
Citations number
52
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON
ISSN journal
00404020 → ACNP
Volume
55
Issue
51
Year of publication
1999
Pages
14649 - 14664
Database
ISI
SICI code
0040-4020(199912)55:51<14649:SO3SFC>2.0.ZU;2-D
Abstract
Cyclic sulfates 21-23 and sulfite 27 derived from glucofuranose lead to the 3,6-anhydrosugar 28 in excellent yields when treated with sodium sulfite o r in basic media. When treated with sodium sulfite, the 3-deoxy derivative 24 fails to give the intramolecular cyclization which leads to the anhydros ugars. Instead it gives the disulfonate derivative 26. 28 was used as start ing material to prepare bicyclonucleosides 43 and 46, which are analogues o f the anti-HIV agents ddC and ddA. (C) 1999 Elsevier Science Ltd. All right s reserved.