Synthesis of 2-Deoxy-4-thio-D-ribofuranose and Its 3-Azido Analogue from L-Arabinose; Intermediates in the Synthesis of 4′-Thiodeoxynucleosides

References

• Mitsuya , H. and Broder , S. 1986 . Proc. Natl. Acad. Sci. USA , 83 : 1911 – 1915 .
   PubMed Web of Science ®Google Scholar
• Mitsuya , H. , Weinhold , K. , Furman , P. A. , Clair , M. H. St. , Lehrman , S. N. , Gallo , R. C. , Bolognesi , D. , Barry , D. W. and Broder , S. 1985 . Proc. Natl. Acad. Sci. USA , 82 : 7096 – 7100 .
   PubMed Web of Science ®Google Scholar
• Balzarini , J. , Kang , G.-J. , Dalal , M. , Herdewljn , P. , De Clercq , E. , Broder , S. and Johns , D. G. 1987 . Mol. Pharmacol. , 32 : 162 – 167 .
   PubMed Web of Science ®Google Scholar
• Hamamoto , Y. , Nakashima , H. , Matsui , T. , Matsuda , A. , Ueda , T. and Yamamoto , N. 1987 . Antimicrob. Agents Chemother. , 31 : 907 – 910 .
   PubMed Web of Science ®Google Scholar
• Lin , T.-S. , Guo , J.-Y. , Schinazi , R. F. , Chu , C. K. , Xiang , J.-N. and Prusoff , W. H. 1988 . J. Med. Chem. , 31 : 336 – 340 .
   PubMed Web of Science ®Google Scholar
• Parks , R. E. , Stoeckler , J. D. , Cambor , C. , Savarese , T. M. , Crabtree , G. W. and Chu , S.-H. 1981 . Molecular Actions and Targets for Cancer Chemotherapeutic Agents , Edited by: Sartorelli , A. C. and Bertino , J. S. New York : Academic Press .
   Google Scholar
• Secrist , J. A. , Tiwari , K. N. , Riordan , J. M. and Montgomery , J. A. 1991 . J. Med. Chem. , 34 : 2361 – 2366 .
   PubMed Web of Science ®Google Scholar
• Bellon , L. , Morvan , F. , Barascut , J.-L. and Imbach , J.-L. 1992 . Biophys. Biochem. Res. Commun. , 18 : 797 – 803 .
   Google Scholar
• Bellon , L. , Barascut , J.-L. , Maury , G. , Divita , G. , Goody , R. and Imbach , J.-L. 1993 . Nucleic Acids Res. , 21 : 1587 – 1593 .
   PubMed Web of Science ®Google Scholar
• Huryn , D. M. and Okabe , M. 1992 . Chem. Rev. , 92 : 1745 – 1768 .
   Web of Science ®Google Scholar
• Nayak , U. G. and Whistler , R. L. 1970 . Liebigs Ann. Chem. , 741 : 131 – 138 .
   Google Scholar
• Fu , Y.-L. and Bobek , M. 1976 . J. Org. Chem. , 41 : 3831 – 3834 .
   PubMed Web of Science ®Google Scholar
• Dyson , M. R. , Coe , P. L. and Walker , R. T. 1991 . Carbohydr. Res. , 216 : 237 – 248 .
   Web of Science ®Google Scholar
• Dyson , M. R. , Coe , P. L. and Walker , R. T. 1991 . J. Med. Chem. , 34 : 2782 – 2786 .
   PubMed Web of Science ®Google Scholar
• Secrist , J. A. , Riggs , R. M. , Tiwari , K. N. and Montgomery , J. A. 1992 . J. Med. Chem. , 35 : 533 – 538 .
   PubMed Web of Science ®Google Scholar
• Tber , B. , Fahmi , N. , Ronco , G. , Mackenzie , G. , Villa , P. and Ville , G. 1993 . Collect. Czech. Chem., Commun. , 58 : 18 – 21 .
   Google Scholar
• Uenishi , J. , Motoyama , M. , Nishiyama , Y. and Wakayabashi , S. 1991 . J. Chem. Soc., Chem. Commun. , : 1421 – 1422 .
   Google Scholar
• Wong , M. Y. H. and Gray , G. R. 1978 . J. Am. Chem. Soc. , 100 : 3548 – 3553 .
   Web of Science ®Google Scholar
• Mitsunobu , O. 1981 . Synthesis , : 1 – 28 .
   Web of Science ®Google Scholar
• Blumberg , K. , Fucello , A. and Van Es , T. 1979 . Carbohydr. Res. , 70 : 217 – 232 .
   Web of Science ®Google Scholar