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aÇÒ¸èÇÒÐÐa: ½ð±Ò+10, ¡ïÓаïÖú, лл£¡ 2014-07-25 12:59:24
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aÇÒ¸èÇÒÐÐa: ½ð±Ò+10, ¡ïÓаïÖú, лл£¡ 2014-07-25 12:59:24
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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£º¹²²éµ½215¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 4-fluoro-N,N-dimethyl-2-(4-methyl-2-nitrophenylthio)-benzamide ÏàËÆ¶È:62.5% Bioorganic & Medicinal Chemistry 2010 18 236-241 Synthesis and in vitro evaluation of fluorinated diphenyloxide derivatives and sulfur analogs as serotonin transporter ligands Sylvie Mavel, Nathalie Meheux, Denis Guilloteau, Patrick Emond Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 2-chloro-3,7-dihydroxy-1,9-dimethyldibenzofuran C14H11ClO3 ÏàËÆ¶È:56.2% Phytochemistry 2001 58 1129-1134 Dibenzofurans from the cultured lichen mycobionts of Lecanora cinereocarnea Takao Tanahashi, Yukiko Takenaka, Naotaka Nagakura, Nobuo Hamada Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 2-chloro-7-hydroxy-3-methoxy-1,9-dimethyldibenzofuran C15H13ClO3 ÏàËÆ¶È:56.2% Phytochemistry 2001 58 1129-1134 Dibenzofurans from the cultured lichen mycobionts of Lecanora cinereocarnea Takao Tanahashi, Yukiko Takenaka, Naotaka Nagakura, Nobuo Hamada Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (+)-(S)-methyl dihydroaeruginoic acid C11H11NO3S ÏàËÆ¶È:56.2% Journal of Natural Products 1994 Vol 57 1200 (+)-(S)-Dihydroaeruginoic Acid, an Inhibitor of Septoria tritici and Other Phytopathogenic Fungi and Bacteria, Produced by Pseudomonas fluorescens Ranit Carmi, Shmuel Carmeli, Edna Levy, Francis J. Gough Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . PIPER2 C38H24N4O4 ÏàËÆ¶È:56.2% Bioorganic & Medicinal Chemistry Letters 2002 12 2527-2533 Perylene diimides with different side chains are selective in inducing different G-Quadruplex DNA structures and in inhibiting telomerase Luigi Rossetti, Marco Franceschin, Armandodoriano Bianco, Giancarlo Ortaggi, Maria Savino Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 4-fluoro-AF4 ÏàËÆ¶È:56.2% Magnetic Resonance in Chemistry 2009 47 313-321 Mono- and difluorinated 1, 1, 2, 2, 9, 9, 10, 10-octafluoro[2.2]paracyclophanes (AF4s)¡ªA 1H and 19F NMR study (pages 313¨C321) Ion Ghiviriga, Florian Dulong and William R. Dolbier Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 8-cyanomethyl-6-methyl-2-(2-thienyl)-4H-1-benzopyran-4-one ÏàËÆ¶È:56.2% Archiv der Pharmazie 1996 329 489-497 Synthesis and Antitumour Activity of New Derivatives of Flavone-8-acetic Acid (FAA). Part 1: 6-Methyl Derivatives R. Alan Aitkena, Michael C. Bibby, John A. Double, Roger M. Phillips and Shiv Kumar Sharma Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 2-(2-Chloro-6-fluorobenzyl)malononitrile C10H6ClFN2 ÏàËÆ¶È:56.2% Heterocycles 2011 83 371-383 The Synthesis of Some Derivatives Based on the 4-Benzyl-1H-pyrazole-3,5-diamine Core Luk¨¢š Jedin¨¢k, Vladim¨ªr Kryštof, and Petr Cankař Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 3-(4-Hydroxy-8-methoxy-5H-pyrido[4,3-b]indol-3-yl)propionic acid C15H14N2O4 ÏàËÆ¶È:56.2% Tetrahedron 2012 68 1117-1127 Studies on pyrrolidinones. Synthesis of 4,5-fused-3-hydroxypyridinyl-2-propionic acid derivatives Rufine Aku¨¦-G¨¦du, Daniel Couturier, Jean-Pierre H¨¦nichart, Benoit Rigo, G¨¦rard Sanz, Luc Van Hijfte, Anne Bourry Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 2,3,6,11-tetrahydro-11-oxo-2-thioxothiazolo[5,4-a]acridine C14H8N2OS2 ÏàËÆ¶È:56.2% Heterocycles 2000 53 387-395 Synthesis of New Thiazolo[5,4-a]acridine Derivatives Maxime Robin, Robert Faure, Alain P¨¦richaud, and Jean-Pierre Galy* Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 2-amino-4-(N-tosyl-6'-bromo-3'-indolyl)pyrimidine C19H15N4O2BrS ÏàËÆ¶È:56.2% Heterocycles 2000 53 1489-1498 Synthesis of Indolylpyrimidines via Cross-Coupling of Indolylboronic Acid with Chloropyrimidines: Facile Synthesis of Meridianin D Biao Jiang* and Cai-guang Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 4-(4-((3-fluorophenyl)(hydroxyimino)methyl)pyrimidin-2-ylamino)benzonitrile C18H12FN5O ÏàËÆ¶È:56.2% Bioorganic & Medicinal Chemistry 2010 18 2370-2374 Synthesis and biological evaluation of 4-(hydroxyimino)arylmethyl diarylpyrimidine analogues as potential non-nucleoside reverse transcriptase inhibitors against HIV Xiao-Qing Feng, Zhao-Sen Zeng, Yong-Hong Liang, Fen-Er Chen, Christophe Pannecouque, Jan Balzarini, Erik De Clercq Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 4-amino-2,3',4'-tricyanobiphenyl C15H8N4 ÏàËÆ¶È:56.2% Russian Journal of Organic Chemistry 2011 47 1240-1246 Synthesis of 2,3¡ä,4¡ä-tricyanobiphenyl derivatives and tetraphenylphthalocyanines based thereon G. A. Selivanova, E. V. Amosov, L. I. Goryunov, S. V. Balina and V. G. Vasil¡¯ev, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 3,3-dimethyl-3Hbenzothienodioxide[3,2-f][1]benzopyrane ÏàËÆ¶È:56.2% Natural Product Communications 2012 7 891-894 Synthesis and Antimicrobial Activities of Some Sulphur Containing Chromene Derivatives Tuba Şerbetçi, Seher Birteksöz, Soizic Prado, Sylvie Michel and François Tillequin Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 2-(3-trifluoromethylphenyl)-3,4-dihydroisoquinolin-2-ium bromide ÏàËÆ¶È:56.2% Chemical & Pharmaceutical Bulletin 2013 69 204-211 Synthesis of 2-Aryl-3,4-dihydroisoquinolin-2-ium Bromides and Their in Vitro Acaricidal Activity against Psoroptes cuniculi Yan-Ni Ma, Xin-Juan Yang, Le Pan, Zhe Hou, Hui-Ling Geng, Xiao-Ping Song, Le Zhou, Fang Miao Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 5-bromo-3-(4-methoxybenzyl)-1H-indole C16H14BrNO ÏàËÆ¶È:56.2% Tetrahedron 2013 69 1166-1174 Acidic-functionalized ionic liquid as an efficient, green, and metal-free catalyst for benzylation of sulfur, nitrogen, and carbon nucleophiles to benzylic alcohols Xue-Qiang Chu, Ran Jiang, Yi Fang, Zheng-Yang Gu, Hua Meng, Shun-Yi Wang, Shun-Jun Ji Structure 13C NMR ̼Æ×Ä£Äâͼ |

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