期刊文献+

Synthesis and Crystal Structure of a New 3-Amino-3-deoxy Derivative from 3-Keto-D-xylose

Synthesis and Crystal Structure of a New 3-Amino-3-deoxy Derivative from 3-Keto-D-xylose
下载PDF
导出
摘要 The title compound 2 was synthesized by the reaction of 3-keto-D-xylose with O-C6H4NH2NH2 and characterized by IR, NMR and HRMS, and its crystal structure was determined by X-ray diffraction analysis. The crystal is of orthorhombic system (C21H22N2O5, Mr = 382.41), space group P2 1 2 1 2 1 with α = 10.140(2), b = 10.802(2), c = 17.840(4) A, β = 90°, V = 1954.1(7)A^3, Z = 4, Dc = 1.300 g/cm^3, F(000) = 808, μ = 0.094 mm^-1, the final R = 0.0354 and wR = 0.0514 for 1924 observed reflections (I 〉 2σ(I)). One intermolecular and one intramolecular hydrogen bonds were found. The absolute configuration of this molecule was confirmed by comparison with that of the original material. The title compound 2 was synthesized by the reaction of 3-keto-D-xylose with O-C6H4NH2NH2 and characterized by IR, NMR and HRMS, and its crystal structure was determined by X-ray diffraction analysis. The crystal is of orthorhombic system (C21H22N2O5, Mr = 382.41), space group P2 1 2 1 2 1 with α = 10.140(2), b = 10.802(2), c = 17.840(4) A, β = 90°, V = 1954.1(7)A^3, Z = 4, Dc = 1.300 g/cm^3, F(000) = 808, μ = 0.094 mm^-1, the final R = 0.0354 and wR = 0.0514 for 1924 observed reflections (I 〉 2σ(I)). One intermolecular and one intramolecular hydrogen bonds were found. The absolute configuration of this molecule was confirmed by comparison with that of the original material.
出处 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2009年第3期291-294,共4页 结构化学(英文)
基金 supported by the National Natural Science Foundation of China (No. 20472075)
关键词 synthesis crystal structure O-PHENYLENEDIAMINE amino sugar synthesis, crystal structure, O-phenylenediamine, amino sugar
  • 相关文献

参考文献12

  • 1Sibi, M. P.; Lu, J.; Edwards, J. J. Org. Chem. 1997, 62, 5864-5872 and References Therein.
  • 2Pelyvas, I. V.; Mormeret, C.; Herczegh, P. Springer: Berlin 1988, pp 123-162.
  • 3Lindberg, B. Carbohydr. Chem. Biochem. 1990, 48,279-318.
  • 4El Khadem, H. S. Anthracycline Antibiotics; Academic Press: New York 1982, pp 1-285.
  • 5de Freitas Filho, J. R.; Srivastava, R. M.; da Silva, W. J. P.; Cottier, L.; Sinoub, D. Carbohydrate Research 2003, 338, 673-680.
  • 6Ji, X. M.; Sun, H. P.; Mo, J.; Liu H. M. Chinese J. Struct. Chem. 2006, 25, 1492-1496.
  • 7Ji, X. M.; Mo, J.; Liu, H. M.; Sun, H. P. Carbohydrate Research 2006, 341,2312-2320.
  • 8Ji, X. M.; Zhang, B.; Fu, Y. H.; Liu, H. M. Journal of Henan Normal UniversiO, (Nat. Sci. Ed) 2007, 1,104-106.
  • 9Walker, J. N.; Start, D. Acta Crystalloger. 1983, A 39, 158-166.
  • 10Sheldrick, G. M. SHELXS97 and SHELXL97, Univesity of Gottingen, Germany 1997.

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部