期刊文献+

Improved Synthesis and Structure of 3-Carboxy-2-pyrazinecarbohydroxamic Acid

Improved Synthesis and Structure of 3-Carboxy-2-pyrazinecarbohydroxamic Acid
下载PDF
导出
摘要 3-Carboxy-2-pyrazinehydroxamic acid was prepared by a one pot reaction starting from pyrazine-2,3-dicarboxylic anhydride with a high yield, and characterized by IR, Mass spectrum, 1H NMR and 13C NMR spectra and single-crystal X-ray diffraction. It crystallizes in triclinic, space group Pī with a=4.8659(10), b=7.4233(15), c=11.602(2), α=96.904(2), β=92.422(3), γ=107.454(2)°, V=395.51(14)3 , Z=2, Dc=1.689g/cm3 , F(000)=208, μ(MoKα)=0.149 mm-1 , the final R=0.0473 and wR=0.1306 for 2853 observed reflections (I〉2σ (I)). A three-dimensional framework was assembled through intermolecular hydrogen bonding between water and 3-carboxy-2-pyrazine-carbohydroxamic acid molecules. 3-Carboxy-2-pyrazinehydroxamic acid was prepared by a one pot reaction starting from pyrazine-2,3-dicarboxylic anhydride with a high yield, and characterized by IR, Mass spectrum, 1H NMR and 13C NMR spectra and single-crystal X-ray diffraction. It crystallizes in triclinic, space group Pī with a=4.8659(10), b=7.4233(15), c=11.602(2), α=96.904(2), β=92.422(3), γ=107.454(2)°, V=395.51(14)3 , Z=2, Dc=1.689g/cm3 , F(000)=208, μ(MoKα)=0.149 mm-1 , the final R=0.0473 and wR=0.1306 for 2853 observed reflections (I〉2σ (I)). A three-dimensional framework was assembled through intermolecular hydrogen bonding between water and 3-carboxy-2-pyrazine-carbohydroxamic acid molecules.
出处 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2013年第3期403-407,共5页 结构化学(英文)
基金 supported by the National Natural Science Foundation of China (No. 20861007) Science Foundation of State Key Laboratory of Structural Chemistry (No. 20100009) Science and Technology Research Projects in Department of Education of Jiangxi Province (No. GJJ08026)
关键词 3-carboxy-2-pyrazinecarbohydroxamic acid pyrazine-2 3-dicarboxylic anhydride crystal structure 3-carboxy-2-pyrazinecarbohydroxamic acid, pyrazine-2,3-dicarboxylic anhydride, crystal structure
  • 相关文献

参考文献2

二级参考文献16

  • 1Royo, S.; Borggraeve, W. M. D.; Peggion, C.; Formaggio, F.; Crisma, M.; Jimenez, A. I.; Cativiela, C.; Toniol C. Turn and helical peptide handedness governed exclusively by side-chain chiral centers. J. Am. Chem. Soc. 2005, 127, 2036-2037.
  • 2Su, G E; Mu, H. T.; Za, D. M.; Zeng, L. M.; Cativiela, C.; Hammer, R. E; Yu, K. B. Stereospecific synthesis of trans-2,3-diaryl substituted 1-aminocyclopropanecarboxylie acid derivatives. Synth. Commun. 2003, 33, 2873-2884.
  • 3Huang, W. Y.; Su, G. F.; Pan, C. X.; Qin, J. K. (1S,2S,3S)-N-(2-(4-chlorophenyl)-1-{N-[2-methyl-1-(N-methylcarbamoyl)propyl]-carbamoyl}-3-phenylcyclopropyl)benzamide. Acta Cryst., E63 2007, 02686-02687.
  • 4Jimenez, A. I.; Cativiela, C.; Aubry, A.; Marraud, M. β-Turn preferences induced by 2,3-methanophenylalanine chirality. J Am. Chem. Soc. 1998, 120, 9452-9459.
  • 5Sheldrick, G M. SHELXS-97, Program for the Solution of Crystal Structures, university of Gottingen, Germany 1997.
  • 6Sheldrick, G. M. SHELXL-97, Program for the Refinement of Crystal Structures, university of Gottingen, Germany 1997.
  • 7Pan, C. X.; Su, G. F.; Huang, W. Y.; Zhang, Y. Synthesis and crystal structure of N-[1-(2-methyl-1-methylcarbamoyl-propyt-carbamoyl)-2,3- -diphenyl-cyclopropyl]-benzamide. Chinese J. Struct. Chem. 2008, 27, 293-296.
  • 8IUPAC-IUB Commission on Biochemical Nomenclature. Abbreviations and symbols for the description of the conformation of polypeptide chains. J. Mol. Biol. 1970, S2, 1-17.
  • 9Richazdaon,J, S. The anatomy and taxonomy of protein structure. Adv. Protein Chem. 1981, 34, 167-339.
  • 10陈华梅,王月红,林海,林华宽.Synthesis and Crystal Structure of 1,2-Bis-(p-nitrophenylsulfonamido)-4,5-dinitrobenzene[J].Chinese Journal of Structural Chemistry,2007,26(9):1027-1032. 被引量:2

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