期刊文献+

Synthesis and Crystal Structure of 2-(N-Cyclohexyl)-imino-1,4-succinic Acid Dihydrate 被引量:2

Synthesis and Crystal Structure of 2-(N-Cyclohexyl)-imino-1,4-succinic Acid Dihydrate
下载PDF
导出
摘要 The title compound, 2-(N-cyclohexyl)-imino-1,4-succinic acid dihydrate 4, has been prepared and structurally determined by X-ray diffraction analysis. Crystal data: monoclinic, space group Cc, a = 7.5790(15), b = 24.860(5), c = 7.1394(14) ?, β = 104.23(3)°, V = 1303.9(4) ?3, C10H21NO6, Mr = 251.28, Z = 4, Dc = 1.280 g/cm3, μ = 0.105 mm-1, F(000) = 544, R = 0.0397 and wR = 0.0918 for 1212 observed reflections with I ≥ 2σ(I). X-ray structure analysis reveals that there exist two intramolecular and six intermolecular hydrogen-bonding interactions in the crystal lattice, which can stabilize the configuration of the α-imino acid dihydrate 4. The title compound, 2-(N-cyclohexyl)-imino-1,4-succinic acid dihydrate 4, has been prepared and structurally determined by X-ray diffraction analysis. Crystal data: monoclinic, space group Cc, a = 7.5790(15), b = 24.860(5), c = 7.1394(14) ?, β = 104.23(3)°, V = 1303.9(4) ?3, C10H21NO6, Mr = 251.28, Z = 4, Dc = 1.280 g/cm3, μ = 0.105 mm-1, F(000) = 544, R = 0.0397 and wR = 0.0918 for 1212 observed reflections with I ≥ 2σ(I). X-ray structure analysis reveals that there exist two intramolecular and six intermolecular hydrogen-bonding interactions in the crystal lattice, which can stabilize the configuration of the α-imino acid dihydrate 4.
出处 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 北大核心 2005年第1期89-93,共5页 结构化学(英文)
基金 Supported by the National Natural Science Foundation of China (No. 29672004)
关键词 methoxybutenolide synthesis α-imino acid crystal structure hydrogen bonding methoxybutenolide, synthesis, α-imino acid, crystal structure, hydrogen bonding
  • 相关文献

参考文献14

  • 1Chen, Q H; Zou, C. Chin. Z Org, Chem. 1994, 14, 1-11.
  • 2Ma, H M; Shao, R L; Ma, Z H; Cheng, J R. Chin. J. Org. Chem. 2000, 20, 454-463.
  • 3Barrett, G C, Amino Acids and Peptides, Cambridge University Press, Cambridge, U.K. 1998.
  • 4Patel, R N. Stereoselective Biocatalysis, Marcel Dekker, Inc., New York 2000.
  • 5Tessari, P; Soeters, P B; Pittoni, G; Tiengo, A. Amino Acid and Protein Metabolism in Health and Disease: Nutritional Implications, Smith-Gordon and Company Ltd., London 1997.
  • 6Cooper, D N. Human Gene Evolution, BIOS Scientific Publishers Ltd, Oxford, U, K. 1999.
  • 7Cantor, C R. Genomics, The Science and Technology behind the Human Genome Project, John Wiley & Sons Inc., New York 1999.
  • 8Collins, A N; Sheldrake, G N; Crosby, J. Chirality in Industry (The Commercial Manufacture and Applications of Opitically Active Compounds), John Wiley & Sons, New York 1992.
  • 9Cardillo, G; Tommasini, C. Chem. Soc. Rev. 1996, 23, 117-128.
  • 10Seebach, D; Gademarm, K; Ernst, M; Hoyer, D. Angew. Chem. int. Ed. Engl. 1999, 38, 1223-1226.

同被引文献8

引证文献2

二级引证文献1

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