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ר¼Ò¾Ñé: +726 - PhEPI: 3
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wawlgch: ½ð±Ò+10, ¡ïÓаïÖú 2013-10-18 14:55:27
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wawlgch: ½ð±Ò+10, ¡ïÓаïÖú 2013-10-18 14:55:27
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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£º¹²²éµ½398¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . benzofuran-2-carboxaldehyde C9H6O2 ÏàËÆ¶È:100% Natural Product Communications 2009 4 1031-1036 Naturally Occurring Labdane Diterpene and Benzofuranfrom Globba pendula Maulidiani, Khozirah Shaari, Christian Paetz, Johnson Stanslas, Faridah Abas andNordin Haji Lajis Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 1H-Indole-3-carboxaldehyde ÏàËÆ¶È:100% 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 . indolyl-3-carbaldehyde ÏàËÆ¶È:88.8% 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 4 . 1H-indole-3-carboxaldehyde ÏàËÆ¶È:88.8% 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 5 . ßÅßá-3-¼×È© ÏàËÆ¶È:88.8% China Journal of Chinese Materia Medica 2012 37 2906-2909 Preliminary study on chemical constituents seperated from Cayratia japonica CUI Chuan-wen; SUN Cui-ling; CHEN Quan-cheng; ZOU Xiu-hong; HUANG Xue-min; CHEN Hai-feng Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 3-formylindole ÏàËÆ¶È:77.7% China Journal of Chinese Materia Medica 2007 32 688-691 Studies on chemical constituents in root of Isatis indigotica ZUO Li, LI Jianbei, XU Jing, YANG Jingzhi, ZHANG Dongming, TONG Yongling Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . [10-2H]Indole-3-carboxaldehyde C9H6HNO ÏàËÆ¶È:77.7% Bioorganic & Medicinal Chemistry 2011 19 1390-1399 Brassinin oxidase mediated transformation of the phytoalexin brassinin:Structure of the elusive co-product, deuterium isotope effect and stereoselectivity M. Soledade C. Pedras, Zoran Minic, Vijay K. Sarma-Mamillapalle Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 3-amino-2-formylimidazo[1,2-a]pyridine C8H7N3O ÏàËÆ¶È:77.7% 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 9 . 3,3¡ä-diformyl-2,2¡ä-biindoyl C18H12N2O2 ÏàËÆ¶È:77.7% Heterocycles 2004 63 2371-2377 Effect of Sodium Naphthalenide, a Key Set Reagent, on 3-Substituted Indoles Avijit Banerji*, Debasish Bandyopadhyay, and Bidyut Basak Structure 13C NMR ̼Æ×Ä£Äâͼ |

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