The 7-bromo derivative of 2-amino-2′-deoxy-tubercidin fluorinated at the sugar moiety

Acta Crystallographica Section C: Crystal Structure Communications

Volumn 63, Issue 10, 2007, Pages

  Seela, Frank ^a   Ding, Ping ^a   Peng, Xiaohua ^a   Eickmeier, Henning ^a   Reuter, Hans ^a  

^a UNIVERSITY OF OSNABRÜCK   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CONFORMATIONS; HYDROGEN BONDS; MOLECULAR STRUCTURE;

SUGAR PUCKER; THREE-DIMENSIONAL NETWORK;

DERIVATIVES;

BROMINE DERIVATIVE; CARBOHYDRATE; DRUG DERIVATIVE; FLUORINE DERIVATIVE; TUBERCIDIN;

ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; HYDROGEN BOND; PROBABILITY; X RAY CRYSTALLOGRAPHY;

BROMINE COMPOUNDS; CARBOHYDRATES; CRYSTALLOGRAPHY, X-RAY; FLUORINE COMPOUNDS; HYDROGEN BONDING; MODELS, MOLECULAR; MOLECULAR STRUCTURE; PROBABILITY; TUBERCIDIN;

ARA;

EID: 34948900318     PISSN: 01082701     EISSN: 01082701     Source Type: Journal    
DOI: 10.1107/S0108270107027138     Document Type: Article

References (20)

1. Altona, C. & Sundaralingam, M. (1972). J. Am. Chem. Soc. 94, 205-212.
2. Bergstrom, D. E., Brattesani, A. J., Ogawa, M. K., Reddy, P. A., Schweickert, M. J., Balzarini, X & De Clercq, E. (1984). J. Med. Chem. 27, 285-292.
3. De Clercq, E., Bergstrom, D. E., Robins, M. J., Montgomery, J. A. & Holy, A. (1986). Antimicrob. Agents Chemother. 29, 482-487.
4. Filler, R. & Naqvi, S. M. (1979). Organofluorine Chemicals and Their Industrial Applications, edited by R. E. Banks & E. Horwood, pp. 123-153. New York: Hoisted Press.
5. Flack, H. D. (1983). Acta Cryst. A39, 876-881.
6. He, J., Mikhailopulo, I. & Seela, F. (2003). J. Org. Chem. 68, 5519-5524.
7. IUPAC-IUB Joint Commission on Biochemical Nomenclature (1983). Eur. J. Biochem. 131, 9-15.
8. Marquez, V. E., Tseng, C K., Mitsuya, H., Aoki, S., Kelley, X. A., Ford, H. Jr, Roth, J. S., Broder, S., Johns, D. G. & Driscoll, J. S. (1990). J. Med. Chem. 33, 978-985.
9. Masood, R., Ahluwalia, G. S., Cooney, D. A., Fridland, A., Marquez, V. E., Driscoll, J. S., Hao, Z., Mitsuya, H., Perno, C. F. & Broder, S. (1990). Mol. Pharmacol. 37, 590-596.
10. Peng, X. & Seela, F. (2004). Org. Biomol Chem. 2, 2838-2846.
11. Ramzaeva, N. & Seela, E (1996). Helv. Chim. Acta, 79, 1549-1558.
12. Seela, F., Chittepu, P., He, Y., He, J. & Xu, K. (2005). Nucleosides Nucleotides Nucleic Acids, 24, 847-850.
13. Seela, F., Peng, X., Eickmeier, H. & Reuter, H. (2006). Acta Cryst. C62, o593-o595.
14. Seela, F., Sirivolu, V. R., He, J. & Eickmeier, H. (2005). Acta Cryst. C61, o67-o69.
15. Seela, F. & Thomas, H. (1995). Helv. Chim. Acta, 78, 94-108.
16. Seela, F., Zulauf, M. & Debelak, H. (2000). Helv. Chim. Acta, 83, 1437-1453.
17. Sheldrick, G. M. (1997). SHELXTL. Release 5.1. Bruker AXS Inc., Madison, Wisconsin, USA.
18. Siemens (1996). XSCANS. Release 2.2. Siemens Analytical X-ray Instruments Inc., Madison, Wisconsin, USA.
19. Spek, A. L. (2003). J. Appl. Cryst. 36, 7-13.
20. Wijk, J. van & Altona, C. (1993). PSEUROT. Version 6.2 of July 1993. University of Leiden, The Netherlands.