{"id":80,"date":"2018-02-28T11:29:17","date_gmt":"2018-02-28T03:29:17","guid":{"rendered":"http:\/\/www.zzuchem.com\/?page_id=80"},"modified":"2018-03-13T12:10:21","modified_gmt":"2018-03-13T04:10:21","slug":"before-2014","status":"publish","type":"page","link":"http:\/\/www.zzuchem.com\/index.php\/publications\/before-2014\/","title":{"rendered":"Before 2014"},"content":{"rendered":"
    \n
  1. \n

    Xu, LI; Xiao-Lan, CHEN; Jin-Wei, YUAN; Hai-Sheng, ZHU; Ling-Bo, QU, Synthesis and Crystal Structure of (E)-2-(1-(2-Hydroxy-4-methoxyphenyl)ethylideneamino)-3-(4-hydroxyphenyl)methyl Propionate. Chinese Journal of Structural Chemistry <\/em>2013,<\/strong> 32<\/em> (5), 751-755.<\/span><\/p>\n<\/li>\n

  2. \n

    Chen, Xiaolan; Li, Xu; Yuan, Jinwei; Qu, Lingbo; Wang, Shaohui; Shi, Hanyu; Tang, Yuchun; Duan, Likun, Simple, efficient one-pot method for synthesis of novel N-attached 1,2,3-triazole containing bisphosphonates. Tetrahedron <\/em>2013,<\/strong> 69<\/em> (20), 4047-4052.<\/span><\/p>\n<\/li>\n

  3. \n

    Zhang, T.; Du, J.; Liu, L.; Chen, X.; Yang, F.; Jin, Q., Inhibitory effects and underlying mechanism of 7-hydroxyflavone phosphate ester in HeLa cells. PLoS One <\/em>2012,<\/strong> 7<\/em> (5), e36652.<\/span><\/p>\n<\/li>\n

  4. \n

    Qu, Zhibo; Chen, Xiaolan; Yuan, Jinwei; Qu, Lingbo; Li, Xu; Wang, Fujun; Ding, Xiling; Zhao, Yufen, CuSO4\u00b75H2O-catalyzed alkynylphosphonates formation \u2014 An efficient coupling reaction of terminal alkynes withH-phosphonates. Can. J. Chem. <\/em>2012,<\/strong> 90<\/em> (9), 747-752.<\/span><\/p>\n<\/li>\n

  5. \n

    Qu, Zhibo; Chen, Xiaolan; Yuan, Jinwei; Bai, Yunliang; Chen, Tong; Qu, Lingbo; Wang, Fujun; Li, Xu; Zhao, Yufen, New synthetic methodology leading to a series of novel heterocyclic \u03b1-aminophosphonates: a very attractive expansion of Kabachnik\u2013Fields reaction. Tetrahedron <\/em>2012,<\/strong> 68<\/em> (15), 3156-3159.<\/span><\/p>\n<\/li>\n

  6. \n

    Qu, Zhibo; Chen, Xiaolan; Wei, Donghui; Ke, Diandian; Qu, Lingbo; Yuan, Jinwei; Bai, Yunliang; Wang, Fujun; Zhao, Yufen, A DFT study of the enantioselective reduction of oxime ethers promoted by chiral spiroborate esters. Int. J. Quantum Chem <\/em>2012,<\/strong> 112<\/em> (5), 1449-1459.<\/span><\/p>\n<\/li>\n

  7. \n

    Chen, Xiaolan; Yuan, Jinwei; Qu, Lingbo; Qu, Zhibo; Xu, Shaohua; Wang, Fujun; Zhao, Yufen, Synthesis and Spectroscopic Characterization of Some New Piperazine Phosphoramide Derivatives of 4-Hydroxycoumarin. Phosphorus Sulfur <\/em>2012,<\/strong> 187<\/em> (2), 245-254.<\/span><\/p>\n<\/li>\n

  8. \n

    \u4e8e\u5c9a\u5c9a; \u9648\u6653\u82f1; \u5f20\u5b88\u4ec1; \u9648\u6653\u5c9a; \u6768\u5189; \u5c48\u51cc\u6ce2, \u5149\u8c31\u6cd5\u7814\u7a76\u9178\u5ea6\u5bf9\u4e00\u79cd\u767d\u6768\u7d20\u884d\u751f\u7269\u4e0e\u725b\u8840\u6e05\u767d\u86cb\u767d\u76f8\u4e92\u4f5c\u7528\u7684\u5f71\u54cd. \u5149\u8c31\u5b9e\u9a8c\u5ba4<\/em>2011,<\/strong> 28<\/em> (4), 2120-2127.<\/span><\/p>\n<\/li>\n

  9. \n

    Jiang, Yuqin; Chen, Xiaolan; Qu, Lingbo; Wang, Junliang; Yuan, Jinwei; Chen, Senshen; Li, Xu, An Efficient Ultrasound-assisted Method for the Synthesis of 1,4-Disubstituted Triazoles. Z. Naturforsch <\/em>2011,<\/strong> 66b<\/em>, 77-82.<\/span><\/p>\n<\/li>\n

  10. \n

    Jiang, Y.; Chen, X.; Qu, L.; Wang, J.; Yuan, J.; Chen, S.; Li, X.; Qu, C., Ultrasonic-assisted synthesis of chrysin derivatives linked with 1,2,3-triazoles by 1,3-dipolar cycloaddition reaction. Ultrason. Sonochem. <\/em>2011,<\/strong> 18<\/em> (2), 527-33.<\/span><\/p>\n<\/li>\n

  11. \n

    \u59dc\u7389\u94a6; \u9648\u6653\u5c9a; \u5c48\u51cc\u6ce2; \u738b\u4fca\u4eae; \u8881\u91d1\u4f1f; \u6731\u6d77\u751f, \u76d0\u9178\u6797\u53ef\u9709\u7d20\u7684\u6838\u78c1\u5171\u632f\u7814\u7a76. \u6cb3\u5357\u5e08\u8303\u5927\u5b66\u5b66\u62a5(\u81ea\u7136\u79d1\u5b66\u7248) <\/em>2010,<\/strong> 38<\/em> (4), 88-94.<\/span><\/p>\n<\/li>\n

  12. \n

    \u9648\u6653\u5c9a; \u5f90\u5c11\u534e; \u674e\u9521\u52c7; \u5c48\u51cc\u6ce2; \u738b\u4fca\u4eae; \u8881\u91d1\u4f1f; \u674e\u4f1a\u5a1c, 6-\u785d\u57fa_7_\u4e8c\u5f02\u4e19\u57fa\u9999\u8c46\u7d20\u78f7\u9178\u916f\u7684\u7ed3\u6784\u786e\u5b9a. \u6ce2\u8c31\u5b66\u6742\u5fd7<\/em>2010,<\/strong> 27<\/em> (4), 635-641.<\/span><\/p>\n<\/li>\n

  13. \n

    Chen, Xiao-Lan; Qu, Zhi-Bo; Li, Xi-Yong; Jiang, Yu-Qin; Qu, Ling-Bo; Yuan, Jin-Wei, Synthesis of New Types of N-Arylpiperazine Phosphoramide Analogues of Chrysin. J. Chin. Chem. Soc. <\/em>2010,<\/strong> 57<\/em>, 144-148.<\/span><\/p>\n<\/li>\n

  14. \n

    Chen, Xiaolan; Jinwei Yuan; Junliang Wang; Lingbo Qu; Zhangqi Yu; Zhao, Yufen, A convenient synthesis of chrysin-7-yl aryl N-bis(2-chloroethyl)phosphoramidate. J. Chem. Res. <\/em>2010<\/strong>, 407-409.<\/span><\/p>\n<\/li>\n

  15. \n

    Qu, Zhibo; Chen, Xiaolan; Qu, Lingbo; Yuan, Jinwei; Li, Huina; Zhao, Yufen, Synthesis of Novel Piperazine Phosphoramidate Analogues of 2-Arylquinolones. Phosphorus Sulfur <\/em>2010,<\/strong> 185<\/em> (7), 1516-1520.<\/span><\/p>\n<\/li>\n

  16. \n

    Qu, Zhibo; Chen, Xiaolan; Qu, Chen; Qu, Lingbo; Yuan, Jinwei; Wei, Donghui; Li, Huina; Huang, Xiaoying; Jiang, Yuqin; Zhao, Yufen, Fragmentation pathways of eight nitrogen-containing bisphosphonates (BPs) investigated by ESI-MSn in negative ion mode. Int. J. Mass spectrom. <\/em>2010,<\/strong> 295<\/em> (1-2), 85-93.<\/span><\/p>\n<\/li>\n

  17. \n

    CHEN Xiao-Lan; YUAN Jin-Wei; QU Zhi-Bo; YU Zhang-Qi; QU Ling-Bo; Yu-Fen, ZHAO, Synthesis and Crystal Structure of Diisopropyl Genistein-7-yl Phosphate. \u7ed3\u6784\u5316\u5b66<\/em>2010,<\/strong> 29<\/em> (11), 1676-1679.<\/span><\/p>\n<\/li>\n

  18. \n

    Chen, Xiaolan; Zhou, Yadong; Qu, Lingbo; Liu, Xiangqian; Yuan, Jinwei; Zhao, Yufen, Synthesis of Novel Coumarin-7,8-cyclophosphoramide Analogs. Synth. Commun. <\/em>2010,<\/strong> 40<\/em> (13), 1992-1997.<\/span><\/p>\n<\/li>\n

  19. \n

    Chen, Xiaolan; Yuan, Jinwei; Zhang, Shouren; Qu, Lingbo; Zhao, Yufen, Synthesis of the Novel Phosphoramidate Derivatives of Chrysin. Phosphorus Sulfur <\/em>2010,<\/strong> 185<\/em> (2), 274-278.<\/span><\/p>\n<\/li>\n

  20. \n

    \u8881\u91d1\u4f1f; \u5c48\u51cc\u6ce2; \u9648\u6653\u5c9a; \u674e\u6587\u950b; \u8d75\u7389\u82ac, ESI\u8d28\u8c31\u6cd5\u5bf9\u9ec4\u916e-7-\u78f7\u9170\u5316\u6c28\u57fa\u9178\u916f\u4e0e\u6eb6\u83cc\u9176\u76f8\u4e92\u4f5c\u7528\u7684\u7814\u7a76. \u5206\u6790\u6d4b\u8bd5\u5b66\u62a5<\/em>2009,<\/strong> 28<\/em> (2), 135-139.<\/span><\/p>\n<\/li>\n

  21. \n

    \u8881\u91d1\u4f1f; \u9648\u6653\u5c9a; \u5c48\u51cc\u6ce2; \u5c48\u667a\u535a; \u5362\u5efa\u838e; \u8d75\u7389\u82ac, \u4e00\u79cd\u65b0\u578b\u7684\u55b9\u5549\u6c28\u57fa\u78f7\u9178\u916f\u884d\u751f\u7269\u7684\u6ce2\u8c31\u5b66\u7814\u7a76. \u6ce2\u8c31\u5b66\u6742\u5fd7  Chinese Journal of Magnetic Resonance <\/em>2009,<\/strong> 26<\/em> (1), 95-102.<\/span><\/p>\n<\/li>\n

  22. \n

    \u5c48\u667a\u535a; \u9648\u6653\u5c9a; \u5c48\u51cc\u6ce2; \u8881\u91d1\u4f1f; \u5362\u5efa\u838e; \u8d75\u7389\u82ac, \u963f\u666e\u5511\u4ed1\u7684\u6ce2\u8c31\u5b66\u6570\u636e\u548c\u7ed3\u6784\u786e\u8bc1. \u6ce2\u8c31\u5b66\u6742\u5fd7<\/em>2009,<\/strong> 26<\/em> (2), 272-278.<\/span><\/p>\n<\/li>\n

  23. \n

    \u9648\u6653\u5c9a; \u5468\u4e9a\u4e1c; \u8881\u91d1\u4f1f; \u5c48\u51cc\u6ce2; \u5218\u5411\u524d; \u8d75\u7389\u82ac, \u65b0\u578b\u9999\u8c46\u7d20-7-8-\u73af\u78f7\u9170\u80fa\u884d\u751f\u7269\u7684\u5408\u6210\u4e0eNMR\u7814\u7a76. \u6ce2\u8c31\u5b66\u6742\u5fd7<\/em>2009,<\/strong> 26<\/em> (3), 301-307.<\/span><\/p>\n<\/li>\n

  24. \n

    \u9648\u6653\u5c9a; \u5f20\u5b88\u4ec1; \u5c48\u51cc\u6ce2; \u67f3\u4e43\u65b9; \u8d75\u7389\u82ac, \u65b0\u578b\u767d\u6768\u7d20-7-\u6c28\u57fa\u78f7\u9178\u916f\u884d\u751f\u7269\u7684\u5408\u6210\u4e0e\u6ce2\u8c31\u5b66\u7814\u7a76. \u6ce2\u8c31\u5b66\u6742\u5fd7<\/em>2009,<\/strong> 26<\/em> (2), 239-246.<\/span><\/p>\n<\/li>\n

  25. \n

    \u9648\u6653\u5c9a; \u674e\u6167; \u8881\u91d1\u4f1f; \u5c48\u51cc\u6ce2; \u5218\u5411\u524d; \u8d75\u7389\u82ac, ESIMS\u7814\u7a76\u9ec4\u916e\u542b\u78f7\u884d\u751f\u7269\u4e0e\u6eb6\u83cc\u9176\u7684\u7ade\u4e89\u4f5c\u7528. \u90d1\u5dde\u5927\u5b66\u5b66\u62a5<\/em>2009,<\/strong> 30<\/em> (3), 106-109.<\/span><\/p>\n<\/li>\n

  26. \n

    Jin-Wei, YUAN; Xiao-Lan, CHEN; Ling-Bo, QU; Yu, ZHU; Xiao-Ying, HUANG; Yu-Fen, ZHAO, Synthesis and Crystal Structure of 5,7-Dimethoxy-2-phenylquinolin-4-yl Phenyloxy (N-L-Alanine ethyl ester Phosphoramidate. \u7ed3\u6784\u5316\u5b66 <\/em>2009,<\/strong> 28<\/em> (4), 498-502.<\/span><\/p>\n<\/li>\n

  27. \n

    Yuan, Jinwei; Chen, Xiaolan; Qu, Lingbo; Zhang, Shouren; Lu, Jiansha; Zhao, Yufen, A Convenient Synthesis of Novel Phosphoramide Mustard Analogues of 2-Arylquinolone. Phosphorus Sulfur <\/em>2009,<\/strong> 184<\/em> (11), 2936-2944.<\/span><\/p>\n<\/li>\n

  28. \n

    Yuan, Jin-Wei; Qu, Zhi-Bo; Chen, Xiao-Lan; Zhou, Ya-Dong; Qua, Ling-Bo; Zhao, Yu-Fen, Synthesis of a Novel Type of Phosphoramidate Derivatives of 2-Arylquinolone. J. Chin. Chem. Soc. <\/em>2009,<\/strong> 56<\/em>, 51-58.<\/span><\/p>\n<\/li>\n

  29. \n

    \u8881\u91d1\u4f1f; \u9648\u6653\u5c9a; \u5c48\u51cc\u6ce2; \u7b80\u671d\u661f; \u8d75\u7389\u82ac, \u514b\u6797\u9709\u7d20\u78f7\u9178\u916f\u7684\u6ce2\u8c31\u5b66\u7814\u7a76. \u6ce2\u666e\u5b66\u6742\u5fd7 <\/em>2008,<\/strong> 25<\/em> (4), 523-530.<\/span><\/p>\n<\/li>\n

  30. \n

    \u9648\u6653\u5c9a; \u6bb5\u6625\u5efa; \u674e\u5fd7; \u5218\u82e5\u96e8; \u5c48\u51cc\u6ce2; \u8d75\u7389\u82ac, \u5c3f\u82f75-\u4f4d\u78f7\u9170\u80fa\u7684\u5408\u6210\u53ca\u7535\u55b7\u96fe\u7535\u79bb\u8d28\u8c31\u7814\u7a76. \u5206\u6790\u6d4b\u8bd5\u5b66\u62a5 <\/em>2008,<\/strong> 27<\/em> (8), 839-843.<\/span><\/p>\n<\/li>\n

  31. \n

    Liuji, Zhang; Lingbo, Qu; Baojun, Zhang; Xiaolan, Chen; Yufen, Zhao, A Convenient Method for the Synthesis of Cyclophosphamide Analogues. Phosphorus Sulfur <\/em>2008,<\/strong> 183<\/em> (2-3), 799-803.<\/span><\/p>\n<\/li>\n

  32. \n

    Lingbo, Qu; Xiaona, Shi; Xiaolan, Chen; Libo, Fan, Synthesis of Solanesyl Phosphonate. Phosphorus Sulfur <\/em>2008,<\/strong> 183<\/em> (2-3), 631-635.<\/span><\/p>\n<\/li>\n

  33. \n

    Kashemirov, B. A.; Bala, J. L.; Chen, X.; Ebetino, F. H.; Xia, Z.; Russell, R. G.; Coxon, F. P.; Roelofs, A. J.; Rogers, M. J.; McKenna, C. E., Fluorescently labeled risedronate and related analogues: "magic linker" synthesis. Bioconjug Chem <\/em>2008,<\/strong> 19<\/em> (12), 2308-10.<\/span><\/p>\n<\/li>\n

  34. \n

    Chen, Xiaolan; Shi, Xiaona; Qu, Lingbo; Yuan, Jinwei; Zhao, Yufen, ESI Investigation of Non-Covalent Complexes between Phosphorylated Daidzein Derivatives and Insulin. Phosphorus Sulfur <\/em>2008,<\/strong> 183<\/em> (2-3), 527-537.<\/span><\/p>\n<\/li>\n

  35. \n

    Chen, Xiaolan; Qu, Lingbo; Li, Wenfeng; Yuan, Jinwei; Zhao, Yufen, Synthesis of Phosphoryl Amino Acids Chrysin Esters. Phosphorus Sulfur <\/em>2008,<\/strong> 183<\/em> (2-3), 603-609.<\/span><\/p>\n<\/li>\n

  36. \n

    \u5c48\u51cc\u6ce2; \u90c1\u6709\u795d; \u90ed\u7389\u534e; \u9648\u6653\u5c9a, \u8367\u5149\u5149\u8c31\u6cd5\u7814\u7a76\u78f7\u9170\u53165,7-\u4e8c\u7f9f\u57fa\u9ec4\u916e\u4e0ectDNA\u7684\u76f8\u4e92\u4f5c\u7528. \u5206\u6790\u6d4b\u8bd5\u5b66\u62a5<\/em>2007,<\/strong> 26<\/em> (5), 651-654.<\/span><\/p>\n<\/li>\n

  37. \n

    \u5c48\u51cc\u6ce2; \u738b\u73b2; \u9648\u6653\u5c9a; \u8881\u91d1\u4f1f; \u6768\u5189; \u674e\u840d, \u845b\u6839\u7d20\u53ca\u5176\u884d\u751f\u7269\u4e0e\u725b\u8840\u6e05\u767d\u86cb\u767d\u76f8\u4e92\u4f5c\u7528\u7814\u7a76. \u5316\u5b66\u5b66\u62a5<\/em>2007,<\/strong> 65<\/em> (21), 2417-2422.<\/span><\/p>\n<\/li>\n

  38. \n

    \u9648\u6653\u5c9a, \u90c1\u7ae0\u7426, \u5c48\u51cc\u6ce2, \u8881\u91d1\u4f1f, \u5362\u5efa\u838e, \u8d75\u7389\u82ac, \u67d3\u6599\u6728\u7d20\u7684\u78f7\u9170\u5316\u7ed3\u6784\u6539\u9020\u53ca\u4e0e\u6eb6\u83cc\u9176\u7684\u5f31\u76f8\u4e92\u4f5c\u7528. \u836f\u5b66\u5b66\u62a5 <\/em>2007,<\/strong> 42<\/em> (4), 396-400.<\/span><\/p>\n<\/li>\n

  39. \n

    \u9648\u6653\u5c9a, \u77f3\u6653\u5a1c, \u5c48\u51cc\u6ce2, \u8881\u91d1\u4f1f, \u5362\u5efa\u838e, \u8d75\u7389\u82ac, \u5927\u8c46\u82f7\u5143\u78f7\u9170\u5316\u4ea7\u7269\u7684\u7ed3\u6784\u786e\u5b9a. \u6ce2\u8c31\u5b66\u6742\u5fd7 <\/em>2007,<\/strong> 24<\/em> (1), 85-90.<\/span><\/p>\n<\/li>\n

  40. \n

    Xiao-Lan Chen, Ling-Bo Qu, Jin-Wei Yuan, and Yu-Fen Zhao, Synthesis of a Novel Type of Phosphates of Puerarin. Journal of the Chinese Chemical Society, <\/em>2007,<\/strong> 54<\/em>, 583-585.<\/span><\/p>\n<\/li>\n

  41. \n

    QU, Ling-Bo, CHEN, Xiao-Lan, WANG, Ling, YANG, Ran, ZENG, Hua-Jin, Investigation of the Interaction between Isoflavonoids and Bovine Serum Albumin by Fluorescence Spectroscopy. Chin. J. Chem . <\/em>2007,<\/strong> 25<\/em>, 1151-1155.<\/span><\/p>\n<\/li>\n

  42. \n

    CHEN, Xiao-Lan, YUAN, Jin-Wei, SHI, Xiao-Na, LU, Jian-Sha, QU, Ling-Bo, ZHAO, Yu-Fen, Synthesis of Novel Phosphorylated Daidzein Derivatives and ESI Investigation on Their Non-Covalent Complexes with Lysozyme. Chin. J. Chem . <\/em>2007,<\/strong> 25<\/em>, 1008-1013.<\/span><\/p>\n<\/li>\n

  43. \n

    \u5434\u5efa\u4e3d, \u9648\u6653\u5c9a, \u5c48\u51cc\u6ce2, \u5362\u5efa\u838e, \u8d75\u7389\u82ac, \u03b1-\u4e73\u767d\u86cb\u767d\u4e0e\u78f7\u9170\u5316\u9ec4\u916e\u5f31\u76f8\u4e92\u4f5c\u7528ESI\u8d28\u8c31\u7814\u7a76. \u5206\u6790\u6d4b\u8bd5\u5b66\u62a5 <\/em>2006,<\/strong> 25<\/em> (3), 22-26.<\/span><\/p>\n<\/li>\n

  44. \n

    \u90ed\u7389\u534e, \u9648\u6653\u5c9a, \u5f20\u5a77, \u5c48\u51cc\u6ce2, \u8d75\u7389\u82ac, \u90c1\u6709\u795d, 7-\u7f9f\u57fa\u9ec4\u916e\u53ca\u78f7\u9170\u53167-\u7f9f\u57fa\u9ec4\u916e\u4e0eDNA\u7684\u5f31\u76f8\u4e92\u4f5c\u7528\u8367\u5149\u6cd5\u7814\u7a76. \u6ce2\u8c31\u5b66\u4e0e\u5149\u5b66\u5206\u6790 <\/em>2006,<\/strong> 26<\/em> (3), 475-479.<\/span><\/p>\n<\/li>\n

  45. \n

    YUAN Jin-Wei, CHEN Xiao-Lan, QU Ling-Bo, TANG Ming-Sheng, LIANG Rui-Ling, ZHAO Yu-Fen, A Novel Conformation Investigation on Newly Synthesized Compound of Diethyl Puerarin-7-yl Phosphate. \u7ed3\u6784\u5316\u5b66 <\/em>2006,<\/strong> 25<\/em> (1), 78-84.<\/span><\/p>\n<\/li>\n

  46. \n

    \u8881\u91d1\u4f1f, \u9648\u6653\u5c9a, \u6c6a\u8302\u7530, \u5c48\u51cc\u6ce2, \u8d75\u7389\u82ac, \u845b\u6839\u7d20 7-\u78f7\u9178\u4e8c\u4e59\u916f\u7684NMR\u7814\u7a76. \u6ce2\u8c31\u5b66\u6742\u5fd7 <\/em>2005,<\/strong> 22<\/em> (4), 409-415.<\/span><\/p>\n<\/li>\n

  47. \n

    \u9648\u6653\u5c9a, \u5434\u5efa\u4e3d, \u5362\u5efa\u838e, \u5c48\u51cc\u6ce2, \u8d75\u7389\u82ac, \u4e00\u79cd\u65b0\u7684 4-\u6c28\u57fa\u5b89\u66ff\u6bd4\u6797\u78f7\u9170\u5316\u4ea7\u7269\u7684\u7ed3\u6784\u786e\u5b9a. \u6ce2\u8c31\u5b66\u6742\u5fd7 <\/em>2005,<\/strong> 22<\/em> (2), 209-215.<\/span><\/p>\n<\/li>\n

  48. \n

    Qu Lingbo, Chen Xiaolan, Lu Jiansha,Yuan Jingwei, and Zhao Yufen, CHEMICAL COMPONENTS OF Leptopus chinensis. Chem. Nat. Compd. <\/em>2005,<\/strong> 41<\/em> (5), 565-568.<\/span><\/p>\n<\/li>\n

  49. \n

    CHEN, Xiao-Lana, QU, Ling-Bo, GUO, Lei, LU, Jian-Sha, LIU, Lei, WU, Jian-Lia, Yan, ZHAO, Yu-Fen, Study on the Reaction of Salicylic Acid with Dialkyl Phosphite by NMR and Electrospray Ionization Mass Spectrometry. Chin. J. Chem . <\/em>2005,<\/strong> 23<\/em>, 733-739.<\/span><\/p>\n<\/li>\n

  50. \n

    \u9648\u6653\u5c9a, \u90c1\u6709\u795d, \u5362\u5efa\u838e, \u5ed6\u65b0\u6210, \u9648\u9ece, \u8d75\u7389\u82ac, \u82ef\u4e8c\u915a\u53ca\u6c28\u57fa\u915a\u78f7\u9170\u5316\u884d\u751f\u7269\u7684\u5408\u6210\u53caNMR\u6d4b\u5b9a. \u6ce2\u8c31\u5b66\u6742\u5fd7 <\/em>2004,<\/strong> 21<\/em> (1), 87-91.<\/span><\/p>\n<\/li>\n

  51. \n

    \u9648\u6653\u5c9a, \u4e8e\u6590, \u5c48\u51cc\u6ce2, \u8d75\u7389\u82ac, \u8367\u5149\u53caESI\u8d28\u8c31\u6cd5\u7814\u7a76\u6eb6\u83cc\u9176\u4e0e\u78f7\u9170\u5316\u9ec4\u916e\u7684\u76f8\u4e92\u4f5c\u7528. \u5316\u5b66\u5b66\u62a5 <\/em>2004,<\/strong> 62<\/em> (2), 188-193.<\/span><\/p>\n<\/li>\n

  52. \n

    Zhang, T.; Chen, X.; Qu, L.; Wu, J.; Cui, R.; Zhao, Y., Chrysin and its phosphate ester inhibit cell proliferation and induce apoptosis in Hela cells. Bioorg. Med. Chem. <\/em>2004,<\/strong> 12<\/em> (23), 6097-105.<\/span><\/p>\n<\/li>\n

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    Yan, L.; Xiao-Lan, C.; Juan, H.; Jian-Bo, H.; Ling-Bo, Q.; Yu-Fen, Z., Characterization of novel nucleoside analogs by electrospray ionization mass spectra. Eur J Mass Spectrom (Chichester) <\/em>2004,<\/strong> 10<\/em> (5), 699-703.<\/span><\/p>\n<\/li>\n

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    Liu, H.; Chen, X.; Zhang, S.; Qu, L.; Zhao, Y.; Liu, H.; Dong, M., Separation and determination of dexamethasone sodium phosphate in cochlear perilymph fluid by liquid chromatography with ultraviolet monitoring and electrospray ionization mass spectrometry characterization. J Chromatogr B Analyt Technol Biomed Life Sci <\/em>2004,<\/strong> 805<\/em> (2), 255-60.<\/span><\/p>\n<\/li>\n

  55. \n

    Chen, Xiao-Lan; Qu, Ling-Bo; Zhang, Ting; Liu, Hongxia; Yu, Fei; Yu, You-Zhu; Zhao, Yu-Fen, Direct Observation of Non-covalent Complexes Formed Through Phosphorylated Flavonoid Protein Interaction by Electrospray Ionization Mass Spectrometry. Supramol. Chem. <\/em>2004,<\/strong> 16<\/em> (1), 67-75.<\/span><\/p>\n<\/li>\n

  56. \n

    Chen, Xiao-Lan; Liu, Hong-Xia; Qu, Ling-Bo; Yu, You-Zhu; Lu, Jiansha; Zhao, Yu-Fen, Direct observation of a series of non-covalent complexes formed by phosphorylated flavonoid-protein interactions through electrospray ionization tandem mass spectroscopy. Anal. Chim. Acta <\/em>2004,<\/strong> 511<\/em> (1), 175-182.<\/span><\/p>\n<\/li>\n

  57. \n

    Chen, X. L.; Qu, L. B.; Zhang, T.; Liu, H. X.; Yu, F.; Yu, Y.; Liao, X.; Zhao, Y. F., The nature of phosphorylated chrysin-protein interactions involved in noncovalent complex formation by electrospray ionization mass spectroscopy. Anal. Chem. <\/em>2004,<\/strong> 76<\/em> (1), 211-7.<\/span><\/p>\n<\/li>\n

  58. \n

    Xiaolan, Chen; lingbo, Qu; jiansha, Lu; lei, Guo; youzhu, Yu; yufen, Zhao, Ortho Effects in Bis-phosphoric Esters of the Dihydroxy- and Aminohydroxybenzenes Observed by ESI-MS\/MS. J. Mass Spectrom. Soc. Jpn. <\/em>2004,<\/strong> 52<\/em> (2), 63-67.<\/span><\/p>\n<\/li>\n

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    Chen, Xiaolan; Yu, Youzhu; Qu, Lingbo; Liao, Xincheng; Zhao, Yufen, Synthesis of Novel Phosphoric Esters of Flavone and Isoflavone by Atherton\u2013Todd Reaction. Synth. Commun. <\/em>2004,<\/strong> 34<\/em> (3), 493-499.<\/span><\/p>\n<\/li>\n

  60. \n

    Cao, Shuxia; Su, Yuqian; Yang, Xiaoli; Chen, Xiaolan; Zhao, Yufen, The Investigation of \u03b2\u2010Cyclodextrin Noncovalent Complex with Protein or Dipeptide by Electrospray Ionization Mass Spectrometry. Anal. Lett. <\/em>2004,<\/strong> 37<\/em> (9), 1871-1883.<\/span><\/p>\n<\/li>\n

    @ Copyright Chen Research Group. All Rights Reserved.<\/span><\/p>\n<\/ol>\n","protected":false},"excerpt":{"rendered":"

    Xu, LI; Xiao-Lan, CHEN; Jin-Wei, YUAN; Hai-Sheng, ZHU; … \u7ee7\u7eed\u9605\u8bfb\u201cBefore 2014\u201d<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"parent":49,"menu_order":2,"comment_status":"closed","ping_status":"closed","template":"","meta":[],"_links":{"self":[{"href":"http:\/\/www.zzuchem.com\/index.php\/wp-json\/wp\/v2\/pages\/80"}],"collection":[{"href":"http:\/\/www.zzuchem.com\/index.php\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"http:\/\/www.zzuchem.com\/index.php\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"http:\/\/www.zzuchem.com\/index.php\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.zzuchem.com\/index.php\/wp-json\/wp\/v2\/comments?post=80"}],"version-history":[{"count":7,"href":"http:\/\/www.zzuchem.com\/index.php\/wp-json\/wp\/v2\/pages\/80\/revisions"}],"predecessor-version":[{"id":305,"href":"http:\/\/www.zzuchem.com\/index.php\/wp-json\/wp\/v2\/pages\/80\/revisions\/305"}],"up":[{"embeddable":true,"href":"http:\/\/www.zzuchem.com\/index.php\/wp-json\/wp\/v2\/pages\/49"}],"wp:attachment":[{"href":"http:\/\/www.zzuchem.com\/index.php\/wp-json\/wp\/v2\/media?parent=80"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}