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²éѯ½á¹û£º¹²²éµ½35¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 2-minalin ÏàËÆ¶È:100% China Journal of Chinese Materia Medica 2007 32 1051-1053 Chemical constituents from roots Pseudostellaria heterophylla ZHANG Jian, LI Youbin, WANG Dawei, YIN Zhiqi, DUAN Jinao Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 2-pyrrolecarboxylic acid ÏàËÆ¶È:100% Chinese Journal of Medicinal Chemistry 2011 21 227-231 Study on the secondary metabolites from a marine-derived actinomycete Streptomyces sp£® LI Bin, CHEN Gang, BAI Jiao, PEI Yue-hu* Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . [1.1]-(N,N'',N: N''')-2,2'-Bipyrrolophane ÏàËÆ¶È:80% Helvetica Chimica Acta 1980 63 1190-1197 On the Use of N, N'-Dipyrrolylmethane in Heterocyclic Synthesis. Dipyrrolo [1,2c:2¡ä, 1¡äe]-2 H-imidazole and its Aromatic Anion Ulrich Burger, Francine Dreier Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . Pyrrole-2-carboxylic acid ÏàËÆ¶È:80% Archives of Pharmacal Research 2008 31 1108-1114 GPR12 Selections of the metabolites from an endophytic Streptomyces sp. Asociated with Cistanches deserticola Zhen-Jian Lin, Xiao-Ming Lu, Tian-Jiao Zhu, Yu-Chun Fang and Qian-Qun Gu, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . Z-pyrrole-2-carbaldehyde ÏàËÆ¶È:60% Magnetic Resonance in Chemistry 2010 48 685-692 Study of conformations and hydrogen bonds in the configurational isomers of pyrrole-2-carbaldehyde oxime by 1H, 13C and 15N NMR spectroscopy combined with MP2 and DFT calculations and NBO analysis (pages 685¨C692) Andrei V. Afonin, Igor A. Ushakov, Dmitry V. Pavlov, Andrei V. Ivanov and Al'bina I. Mikhaleva Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 5-hydroxymethyl-2-furaldehyde ÏàËÆ¶È:60% Chinese Journal of Medicinal Chemistry 2007 17 380-382 Chemical constituents from Carthamus tinctorius L. ZHOU Yu-zhi, CHEN Huan, QIAO Li, HAO Dong-fang, HU A Hui-ming, PEI Yue-hu Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 6-chloro-1,2,4,5-tetrahydropyrrolo[3,2,1-hi]indole C10H10NCl ÏàËÆ¶È:60% Heterocycles 2001 54 799-824 3-Aza[5]metacyclophanes: Synthesis and Reactions Daniël S. van Es, Maurice J. van Eis, Stephen N'Krumah, Norbert Gret, Arne Egberts, Marianne de Rijke, Franciscus J. J. de Kanter, Willem H. de Wolf, Friedrich Bickelhaupt,* and Anthony L. Spek Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . p-Hydroxybenzoic acid ÏàËÆ¶È:60% Chemistry of Natural Compounds 2012 48 868-869 Organic acids from Capparis spinosa fruit Quanxia Ren, Wen Chen, Haijiao Zhao, Zengbao Wu, Hua Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . p-hydroxybenzoic acid ÏàËÆ¶È:60% Chinese Traditional and Herbal Drugs 2012 43 1061-1064 Chemical constituents from Sparganii Rhizoma LIANG Qiao-li; KONG Li-juan; WU Qi-nan; Duan Jin-ao Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 2-Amino-5-bromo-3-cyanopyrazine 1-oxide C5H3N4OBr ÏàËÆ¶È:60% Journal of Heterocyclic Chemistry 2012 49 675-677 Synthesis of 3,6-Dibromopyrazine-2,5-dicarbonitrile [1] Nobuhiro Sato and Shunsuke Fukuya Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . vanillic acid ÏàËÆ¶È:50% China Journal of Chinese Materia Medica 2004 29 432-434 Studies on chemical constituents from root of Hedysarum polybotrys HAI Liqian, ZHANG Qiangying, ZHAO Yuying, LIANG Hong, DU Niansheng Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . aldisin C8H8N2O2 ÏàËÆ¶È:50% Journal of Natural Products 1985 Vol 48 47-53 Marine Natural Products: Pyrrololactams from Several Sponges Francis J. Schmitz, Sarath P. Gunasekera, Vijai Lakshmi, L. M. V. Tillekeratne Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . aldisin ÏàËÆ¶È:50% Chemical Research in Chinese Universities 1998 14 426-427 A New Furanolactam from the Chinese Sponge Phacellis Fusca ZENG Long-mei, ZHU Ye, YAN Su-jun and SU Jing-y u Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . aldisin ÏàËÆ¶È:50% Chinese Journal of Marine Drugs 2001 20(1) 9-11 Studies on the chemical constituents of the sponge phakellia fusca thiele LI Wen-lin, MAO Shi-long, YI Yang-hua Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 4,5-dibromopyrrol-2-yl trichloromethyl ketone C6H2Br2Cl3NO ÏàËÆ¶È:50% Organic Letters 2003 Vol. 5, No. 15 2735-2738 Latonduines A and B, New Alkaloids Isolated from the Marine Sponge Stylissa carteri: Structure Elucidation,Synthesis, and Biogenetic Implications Roger G. Linington, David E. Williams, Akbar Tahir, Rob van Soest,and Raymond J. Andersen Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . N,N',N''-tris-(4-methoxyphenyl)-[1,3,5]triazine-2,4,6-triamine C24H24N6O3 ÏàËÆ¶È:50% 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 17 . 2-(E-2-Nitroethenyl)-1H-pyrrole C6H6N2O2 ÏàËÆ¶È:50% Journal of Heterocyclic Chemistry 2005 42 1149-1154 Diels-alder reactions of 2-(2-nitroethenyl)-1H-pyrroles and their oxygen and sulfur analogs with quinones Wayland E. Noland and Gianluca Pardi Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 5-chloro-3-methyl-4H-thieno[3,4-e]-1,2,4-thiadiazine1,1-dioxide ÏàËÆ¶È:50% Journal of Heterocyclic Chemistry 2004 41 45-50 4H-thieno[3,4-e]-and 4H-pyrazolo[4,3-e]-1,2,4-thiadiazine 1,1-dioxides synthesis,chemical properties and evaluation of their Potential Cardiovascular Activity Salvador Vega and Mar¨ªa Esther Arranz Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . compound 3d ÏàËÆ¶È:50% Heterocycles 2003 60 2685-2705 Nuclear Magnetic Resonance Spectroscopical Studies of 2-Carbonyl Derivatives of Five-membered Monoheterocycles and Determination of Aromaticity Indices Kyu Ok Jeon, Ji Sook Yu, and Chang Kiu Lee* Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 5-ôǼ׻ù-2-߻ૼ×È© ÏàËÆ¶È:50% Chinese Traditional and Herbal Drugs 2010 41 201-203 °×¸½×ӵĻ¯Ñ§³É·ÖÑо¿ °¬·ïΰ; ÕÅáÔ; ÀîÑÞ·ï; ÂíÓ¢Àö Structure 13C NMR ̼Æ×Ä£Äâͼ |
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