A Facile and Practical Synthesis of Peracylated 4-Thio-d-ribofuranoses from d-Glucose

Author:

Sun Zhi-Hua1,Wang Bing1

Affiliation:

1. Department of Chemistry, Fudan University, 220 Handan Road, Shanghai 200433, China wangbing@fudan.edu.cn

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Reference34 articles.

1. The synthesis and antiviral activity of some 4'-thio-2'-deoxy nucleoside analogs

2. (a) Parks, R. E., Jr.; Stoeckler, J. D.; Cambor, C.; Savarese, T. M.; Crabtree, G. W.; Chu, S.H. InMolecular Actions and Targets for CancerChemotherapeutic Agents; Sartorelli, A. C., Lazo, J. S., Bertino, J. R., Eds.; Academic Press:  New York, 1981; p 229.

3. (b) Rahim, S. G.; Littler, E.; Powell, K. L.; Collins, P. L.; Dyson, M. R.; Walker, R. T.Proceedings of the31st ICAAC; Chicago, 1991; p 1232.

4. 4′-Thio-RNA: Synthesis of Mixed Base 4′-ThioOligoribonucleotides, Nuclease Resistance, and Base Pairing Properties with Complementary Single and Double Strand

5. 4'-Thio-β-D-oligoribonucleotides: Nuclease Resistance and Hydrogen Bonding Properties

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