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fly2012: ½ð±Ò+20, ¡ïÓаïÖú 2013-04-18 15:06:20
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fly2012: ½ð±Ò+20, ¡ïÓаïÖú 2013-04-18 15:06:20
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1 . Ethyl 4-(sulfooxy)benzoate C9H10O6S ÏàËÆ¶È:77.7% Natural Product Communications 2012 7 47-50 Phytochemical Analysis and Antioxidant Capacity of BM-21, a Bioactive Extract Rich in Polyphenolic Metabolites from the Sea Grass Thalassia testudinum Erik L. Regalado*, Roberto Menendez, Olga Vald¨¦s, Ruth A. Morales, Abilio Laguna,Olivier P. Thomas, Yasnay Hernandez, Clara Nogueiras and Anake Kijjoa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . p-hydroxybenzoic acid ÏàËÆ¶È:66.6% China Journal of Chinese Materia Medica 1999 24 »Æ»¨Ô¶Ö¾»¯Ñ§³É·ÖÑо¿ ÀîÎÄ¿ý¡¡Ð¤Åà¸ù¡¡³ÂÖ¾Á¼¡¡ÁºêØÔÆ¡¡ÑîÏÔÈÙ Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . ethyl 3,4-dihydroxybenzoate C9H10O4 ÏàËÆ¶È:66.6% Chinese Journal of Natural Medicines 2005 3 219-223 Two New Chalcones from the Leaves of Artocarpus heterophyllus YAO Sheng; MIN Zhi-Da Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . p-hydroxy benzoic acid ÏàËÆ¶È:66.6% Natural Product Research and Development 1994 6(3) 4-8 CHEMICAL CONSTITUENTS FROM THE AERIAL PARTS OF EPIMEDIUM KOREANUM NAKAI Li Wenkui; Xiao Peigen Zhang Ruyi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . ethyl-3,4-dihydroxybenzoic acid ÏàËÆ¶È:66.6% Food Chemistry 2007 104 1670-1677 Characterization of antioxidant alkaloids and phenolic acids from anthocyanin-pigmented rice (Oryza sativa cv. Heugjinjubyeo) Ha Sook Chung, Jin Chul Shin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . p-hydroxybenzoic acid ÏàËÆ¶È:66.6% Asian Journal of Traditional Medicines 2006 1 101-104 Several Phenolic Acids from the Fruit of Capparis spinosa Yang Yu , Huiyuan Gao , Zhishu Tang , Xiaomei Song , Lijun Wu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . 5-(4-Fluorophenyl)-7-oxo-1,7-dihydro-[1,2,4]triazolo[4,3-a]-pyrimidine-6-carbonitrile C12H6FN5O ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 2012 60 521-530 Novel Pyrimidinone Derivatives: Synthesis,Antitumor and Antimicrobial Evaluation Azza Taher Taher,and Amira Atef Helwa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . 3-(2-ethoxyphenyl)-4-amino-5-mercapto-4H-1,2,4-triazole ÏàËÆ¶È:60% Journal of Heterocyclic Chemistry 2007 44 1019-1022 Synthesis and crystal structure of novel schiff bases derived from 3-(2-ethoxyphenyl)-4-amino-5-mercapto-4H-1,2,4-triazole San-nu Zhou,Li-xue Zhang,An-jiang Zhang,Ji-shun Sheng and Hai-le Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . 1-(4-(ethoxycarbonyl)phenyl)-1H-pyrazole-3,4-dicarbohydrazide ÏàËÆ¶È:60% Heterocycles 2006 68 733-748 New Efficient Blue-greenish Electroluminescent Materials of 1,3,4-Oxadiazole-based Pyrazole Derivatives En-Ming Chang, Chi-Jen Lin, Fung Fuh Wong,* and Mou-Yung Yeh* Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . 1-phenyl-N3',N4'-dibenzoyl-1H-pyrazole-3,4-dicarbohydrazide ÏàËÆ¶È:60% Heterocycles 2006 68 733-748 New Efficient Blue-greenish Electroluminescent Materials of 1,3,4-Oxadiazole-based Pyrazole Derivatives En-Ming Chang, Chi-Jen Lin, Fung Fuh Wong,* and Mou-Yung Yeh* Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . N1-(4-Hydroxyphenyl)-N2-(methylsulfonyl)-N2-pyrimidin-2-ylglycinamide ÏàËÆ¶È:60% Archiv der Pharmazie 2008 341 690-695 2-Sulfonyliminodihydropyrimidines: A Novel Class of Analgesic Compounds M. Eugenia Gonz¨¢lez-Rosende, Teresa Olivar, Encarna Castillo and Jos¨¦ Sep¨²lveda-Arques Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . ethyl 2-oxo-2,3-dihydro-1H-pyrrolo[2,3-b]pyridine-5-carboxylate C10H10N2O3 ÏàËÆ¶È:60% Heterocycles 2001 55 1583-1590 Synthesis of 5-Substituted 7-Azaoxindoles via Palladium-catalyzed Reactions Mui Cheung,* Robert N. Hunter III, Michael R. Peel, and Karen E. Lackey Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 4-ethoxycarbonyl-2-quinolone ÏàËÆ¶È:58.3% Acta Pharmaceutica Sinica 1990 Vol 25 382-386 STUDIES ON THE CHEMICAL CONSTITUENTS OF BRUCEA JAVANICA (L.) MERR YN Yu and X Li Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . 5-cyano-4-(4-fluoro-phenyl)-6-methyl-pyridine-2-carboxylic acid C14H9FN2O2H ÏàËÆ¶È:58.3% Journal of Heterocyclic Chemistry 2011 48 792-798 A simple, diversity oriented synthesis of highly substituted pyridines Katarzyna Kaczanowska, Holger Eickhoff, Klaus Albert, Karl-Heinz Wiesm¨¹ller and Arnaud-Pierre Schaffner Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . N1-(4-hydroxybenzoyl)-acetamidrazone C9H11N3O2 ÏàËÆ¶È:55.5% Indian Journal of Chemistry 2005 44B 568-572 Reactions of amidines with some carboxylic acid hydrazides Bahçeci,Şule; Y¨¹ksek,Haydar; Serdar,Mevlut Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . 2-Methyl-4-hydroxy-6-oxo-6,7-dihydro-thieno[2,3-b]pyridine-5-carboxylic acid hydroxy amide ÏàËÆ¶È:55.5% Archives of Pharmacal Research 2001 24 270-275 4-Hydroxy-6-Oxo-6,7-Dihydro-Thieno[2,3-b] pyrimidine derivatives: Synthesis and their biological evaluation for the glycine site acting on the N -Methyl-D-aspartate (NMDA) receptor Ki-Jun Hwang, Tae-Suk Lee, Ki-Won Kim, Beom-Tae Kim and Chul-Min Lee, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . p-hydroxy benzoic acid ÏàËÆ¶È:55.5% Journal of Shenyang Pharmaceutical University 2004 21 181-183 Studies on the antibacterial chemical constituents of Senecio cannabifolius Less. (I) WU Bin, WU Li-jun, ZHANG Lei, KIM Chul-sa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . 3-Amino benzoic acid ethyl ester ÏàËÆ¶È:55.5% Archiv der Pharmazie 2008 341 386-392 Synthesis of Platensimycin Analogues and Their Antibiotic Potency J¨¹rgen Krauss, Veronika Knorr, Vera Manhardt, Stefanie Scheffels and Franz Bracher Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . compound 15 ÏàËÆ¶È:55.5% Journal of the Chemical Society, Perkin Transactions 1 1993 2747-2755 2,4-Dihalogenoquinolines. Synthesis, orientation effects and 1H and 13C NMR spectral studies Alan G. Osborne, Jill M. Buley, Helen Clarke, Rachel C. H. Dakin and Paul I. Price Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . 4-hydroxyacetophenone ÏàËÆ¶È:55.5% Journal of the Chemical Society, Perkin Transactions 1 1978 532-539 Extractives from guttiferae. Part 34. Kolaflavanone, a new biflavanone from the nuts of Garcinia kola Heckel. Applications of 13C nuclear magnetic resonance in elucidation of the structures of flavonoids Philip J. Cotterill, Feodor Scheinmann and Ian A. Stenhouse Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-04-17 23:03:16
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1 . Ethyl 4-(sulfooxy)benzoate C9H10O6S ÏàËÆ¶È:77.7% Natural Product Communications 2012 7 47-50 Phytochemical Analysis and Antioxidant Capacity of BM-21, a Bioactive Extract Rich in Polyphenolic Metabolites from the Sea Grass Thalassia testudinum Erik L. Regalado*, Roberto Menendez, Olga Vald¨¦s, Ruth A. Morales, Abilio Laguna,Olivier P. Thomas, Yasnay Hernandez, Clara Nogueiras and Anake Kijjoa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . p-hydroxybenzoic acid ÏàËÆ¶È:66.6% China Journal of Chinese Materia Medica 1999 24 »Æ»¨Ô¶Ö¾»¯Ñ§³É·ÖÑо¿ ÀîÎÄ¿ý¡¡Ð¤Åà¸ù¡¡³ÂÖ¾Á¼¡¡ÁºêØÔÆ¡¡ÑîÏÔÈÙ Structure 13C NMR ̼Æ×Ä£Äâͼ |

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