Dihydroxyacetone (DHA) monomer complexes with CaBr2 and CdCl2

Acta Crystallographica Section C: Crystal Structure Communications

Volumn 64, Issue 3, 2008, Pages

  Slepokura, Katarzyna ^a   Lis, Tadeusz ^a  

^a UNIVERSITY OF WROC AW   (Poland)

Author keywords

[No Author keywords available]

Indexed keywords

ACETONE; CADMIUM COMPOUNDS; CRYSTAL STRUCTURE; DIMERS; HYDROGEN BONDS;

CADMIUM CHLORIDES; KETOSE; MONOMERIC DIHYDROXY ACETONES; WATER MOLECULES;

MONOMERS;

BROMIDE; CADMIUM CHLORIDE; CALCIUM BROMIDE; CALCIUM DERIVATIVE; DIHYDROXYACETONE; DIVALENT CATION;

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

BROMIDES; CADMIUM CHLORIDE; CALCIUM COMPOUNDS; CATIONS, DIVALENT; CRYSTALLOGRAPHY, X-RAY; DIHYDROXYACETONE; DIMERIZATION; HYDROGEN BONDING; MODELS, MOLECULAR; MOLECULAR STRUCTURE;

TETRA;

EID: 40449098792     PISSN: 01082701     EISSN: 01082701     Source Type: Journal    
DOI: 10.1107/S0108270108002527     Document Type: Article

References (25)

1. Allen, F. H. (2002). Acta Cryst. B58, 380-388.
2. Bruker (1997). XP in SHELXTL. Version 5.10. Bruker AXS Inc., Madison, Wisconsin, USA.
3. Davis, L. (1973). Bioorg. Chem. 2, 197-201.
4. Doxsee, K. M., Ferguson, C. M., Wash, P. L. & Saulsbery, R. L. (1993). J. Org. Chem. 58, 7557-7561.
5. Einspahr, H. & Bugg, C. E. (1981). Acta Cryst. B37, 1044-1052.
6. Ferroni, E. L., DiTella, V., Ghanayem, N., Jeske, R., Jodlowski, C., O'Connell, M., Styrsky, J., Svoboda, R., Venkataraman, A. & Winkler, B. M. (1999). J. Org. Chem. 64, 4943-4945.
7. Fessner, W.-D. & Helaine, V. (2001). Curr. Opin. Biotechnol. 12, 574-586.
8. Furneaux, R. H., Gainsford, G. J., Lynch, G. P. & Yorke, S. C. (1993). Tetrahedron, 49, 9605-9612.
9. Gijsen, H. J. M., Qiao, L., Fitz, W. & Wong, C.-H. (1996). Chem. Rev. 96, 443-474.
10. Goodgame, D. M. L., Jeeves, I., Reynolds, C. D. & Skapski, A. C. (1975). Nucleic Acids Res. 2, 1375-1379.
11. Hinkle, P. M., Kinsella, P. A. & Osterhoudt, K. C. (1987). J. Biol. Chem. 262, 16333-16337.
12. Kobayashi, Y., Igarashi, T., Takahashi, H. & Higashi, K. (1976). J. Mol. Struct. 35, 85-99.
13. Koeller, K. M. & Wong, C.-H. (2000). Chem. Rev. 100, 4465-4494.
14. Lambs, L., Reverend, B. D.-L., Kozlowski, H. & Berthon, G. (1988). Inorg. Chem. 27, 3001-3012.
15. Machajewski, T. D. & Wong, C.-H. (2000). Angew. Chem. Int. Ed. 39, 1352-1375.
16. Monder, C., Iohan, F. & Marandici, A. (1988). Steroids, 52, 15-36.
17. Oxford Diffraction (2004). CrysAlis CCD and CrysAlis RED in KM-4 CCD Software. Version 1.171. Oxford Diffraction Poland, Wrocław, Poland.
18. Richardt, G., Federolf, G. & Hebermann, E. (1986). Biochem. Pharmacol. 35, 1331-1335.
19. Senma, M., Taira, Z., Osaki, K. & Taga, T. (1973). J. Chem. Soc. Chem. Commun, pp. 880-881.
20. Sheldrick, G M. (2008). Acta Cryst. A64, 112-122.
21. Ślepokura, K. (2008). Carbohydr. Res. 343, 113-131.
22. Ślepokura, K. & Lis, T. (2004a). Carbohydr. Res. 339, 1995-2007.
23. Ślepokura, K. & Lis, T. (2004b). Acta Cryst. C60, o315-o317.
24. Ślepokura, K. & Lis, T. (2006). Carbohydr. Res. 341, 507-524.
25. Yaylayan, V. A. & Ismail, A. A. (1995). Carbohydr. Res. 276, 253-265.