Synthesis of 1-chloroacetyl-l-dehydroxy-2, 3, 5-tr i-o-benzoyl-β-d-ribofuranose. a potentially versatile intermediate for the synthesis of c-nucleosides

Synthetic Communications

Volumn 22, Issue 19, 1992, Pages 2815-2822

  Han, Hyo Kyung ^a   Lee, Jae Chul ^a   Kim, Joong Hyup ^a   Chi, Dae Yoon ^a   Kang, Yong Han ^b  

^a Korea Institute of Science and Technology   (South Korea)

^b Hanyang University   (South Korea)

Author keywords

[No Author keywords available]

Indexed keywords

C NUCLEOSIDE;

ARTICLE; REACTION ANALYSIS; SYNTHESIS;

EID: 0026785876     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397919208021547     Document Type: Article

References (7)

1. Cornia, M.; Casiraghi, G.; Zetta, L. J. Org. Chem. 1991, 56, 5466 and references therein.
2. Kim, J. H.; Jeon, G.H.; Watanabe, K. A. J. Org. Chem. 1988, 53, 5046.
3. Robins, R. K. Chem. & Enginnering newes 1986, January 27, 28.
4. De Clercq, E. and Walker, R. T. ed. “Antiviral Drug Development; A Multidisciplinary Approach”, Plenum Press, New York, 1987, 28.
5. Pankiewicz, K. W.; Kim, J. H.; Watanabe, K. A. J. Org. Chem. 1985, 50, 3319
6. Wood, S. G.; Dalley, N. K.; George, R. D.; Robins, R. K.; Revankar, G.R. J. Org. Chem. 1984, 49, 3534
7. Wood, S. G.; Dalley, N. K.;George, R. D.; Robins, R. K.; Revankar, G. R. Nucleosides and Nucleoiides. 1984, 3, 187.