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wangwang1989
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qhyy: ½ð±Ò+10 2013-06-20 23:11:38
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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½49¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 4,4',4'-([1,3,5]-triazine-2,4,6-triyltriimino)tribenzoic acid C24H18N6O6 ÏàËÆ¶È:66.6% Journal of Heterocyclic Chemistry 2008 45 533-539 An efficient,¡°green¡± approach to aryl amination of cyanuric chloride using acetic acid as solvent Kirill A. Kolmakov Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 1H-Indole-3-carboxaldehyde ÏàËÆ¶È:66.6% Journal of Agricultural and Food Chemistry 2010 58 12717-12721 Anti-inflammatory Effects of Caper (Capparis spinosa L.) Fruit Aqueous Extract and the Isolation of Main Phytochemicals Haifeng Zhou, Renji Jian, Jie Kang, Xiaoling Huang, Yan Li, Changlong Zhuang, Fang Yang, Lele Zhang, Xiao Fan, Tong Wu, and Xianli Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 1H-indole-3-carboxaldehyde ÏàËÆ¶È:66.6% Chinese Traditional and Herbal Drugs 2012 43 1273-1275 Chemical constituents from rhizomes of Coptis chinensis LI Zhi-feng; WANG Qi; FENG Yu-lin; RAO Yi; YANG Shi-Lin; PEI Yue-hu Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 3-amino-2-formylimidazo[1,2-a]pyridine C8H7N3O ÏàËÆ¶È:62.5% Heterocycles 2005 65 1121-1137 Synthesis of Polyfused Heterocycle Derivatives Containing the Dipyridoimidazole Core by Friedländer's Reaction: Access to Analogs of Ellipticine Nicolas Desbois, Jean-Michel Chezal, Florence Fauvelle, Jean-Claude Debouzy, Claire Lartigue, Alain Gueiffier, Yves Blache, Emmanuel Moreau, Jean-Claude Madelmont, Olivier Chavignon, and Jean-Claude Teulade* Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . indolyl-3-carbaldehyde ÏàËÆ¶È:62.5% Journal of Shenyang Pharmaceutical University 2009 26 430-433 Isolation and identification of chemical constituents of the aerial parts of Salvia chinensis Benth. WANG Ye-ling, LI Zhan-lin, LIU Tao, LIU Hang, HUA Hui-ming Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 1H-indole-3-carbaldehyde ÏàËÆ¶È:62.5% Chinese Journal of Medicinal Chemistry 2012 22 127-130 Isolation and structure identification of chemical constituents from marine bacterium Pantoea agglomerans SHEN Ming-xi; CHEN Gang; LI Wen; MA Hong-mei; FAN Xue-mei; PEI Yue-hu Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 1H-Indole-3-carbaldehyde ÏàËÆ¶È:62.5% Marine Drugs 2013 11 1427-1439 Total Synthesis and Biological Activity of Marine Alkaloid Eudistomins Y1¨CY7 and Their Analogues Huijuan Jin, Puyong Zhang, Krikor Bijian, Sumei Ren, Shengbiao Wan, Moulay A. Alaoui-Jamali and Tao Jiang Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 6-(pyrrol-1-yl)-1,3-dihydro-1-hydroxy-2,1-benzoxaborole ÏàËÆ¶È:57.1% Chinese Chemical Letters 2011 22 1411-1414 Synthesis of a novel pyrrolo-benzoxaborole scaffold and its derivatization via Friedel-Crafts reaction catalyzed by anhydrous stannic chloride Pu Hua Wu,Qing Qing Meng,Hu Chen Zhou Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 2,9-dimethoxy-1,10-phenanthroline ÏàËÆ¶È:57.1% Journal of Heterocyclic Chemistry 2008 45 1167-1170 Facile acidic hydrolysis and displacement reactions of 2-chloro-and 2,9-dichloro-1,10-phenanthroline A. Paul Krapcho and Silvia Sparapani Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 2-(4-Chlorophenyl)-2H-[1,2,3]triazole-4-carbonitrile C9H5ClN4 ÏàËÆ¶È:57.1% Zeitschrift f¨¹r Naturforschung B 2007 62 529-536 Studies with 2-(Arylhydrazono)aldehydes: Synthesis and Chemical Reactivity of Mesoxalaldehyde 2-Arylhydrazones and of Ethyl 2-Arylhydrazono-3-oxopropionates S. Makhseed, H. M. E. Hassaneen, and M. H. Elnagdi Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-06-20 22:52:05
gzl9901
Ìú¸Ëľ³æ (ÎÄ̳¾«Ó¢)
very good
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3Â¥2013-06-20 23:49:39














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