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5Â¥2013-09-30 15:04:52
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karl2100: ½ð±Ò+1, 3Q 2013-10-02 17:05:24
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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£º¹²²éµ½109¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . N-Isobutyl-9-hydroxy-2E,4E-nonadienamide C13H23NO2 ÏàËÆ¶È:58.3% Molecules 2012 17 1425-1436 Total Synthesis and Antidepressant Activities of Laetispicine and Its Derivatives Shuyi Yao,Hui Xie, Li Zhang,Tao Meng, Yongliang Zhang, Xin Wang, Lin Chen,Shengli Pan and Jingkang Shen Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . (tBuO)4-NH2 C40H73N3O10 ÏàËÆ¶È:58.3% European Journal of Organic Chemistry 2010 111-119 A Versatile, Modular Platform for Multivalent Peptide Ligands Based on a Dendritic Wedge Edith H. M. Lempens, Brett A. Helms, Andrea R. Bayles, Maarten Merkx and E. W. Meijer Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . compound 8a ÏàËÆ¶È:57.1% Tetrahedron Letters 2005 46 8711-8714 2-Nitrofurans as dienophiles in Diels-Alder reactions Claudia Della Rosa, Mar¨ªa N. Kneeteman, Pedro M.E. Mancini Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 3-[3,5-Dibromo-4-(9-bromo-2,8-dioxo-1-oxaspiro[4.5]-deca-6,9-dien-7-yloxy)phenyl]propionic acid C18H13Br2BrO6 ÏàËÆ¶È:56.2% Archiv der Pharmazie 2008 341 568-577 Structure-Activity Relationships Study of Bastadin 6,an Anti-Angiogenic Brominated-Tyrosine Derived Metabolite from Marine Sponge Naoyuki Kotoku, Atsushi Hiramatsu, Hiroaki Tsujita, Yoichi Hirakawa, Mami Sanagawa, Shunji Aoki and Motomasa Kobayashi Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . Isohexyl dihydrocaffeate ÏàËÆ¶È:53.8% Phytochemistry 1994 37 1101-1107 Sesquiterpene lactones, lignans and aromatic esters from Cheirolophus species J.Alberto Marco, Juan F. Sanz-Cervera, Vicente Garcia-Lliso, Alfonso Susanna, Nuria Garcia-Jacas Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . (2S)-2-Cyano-pyrrolidine-1-carboxylic acid tert-butyl ester C10H16O2N2 ÏàËÆ¶È:53.8% Canadian Journal of Chemistry 2007 85 85-95 Modular syntheses of oxazolinylamine ligands and characterization of group 10 metal complexes Christine A. Caputo, Florentino d.S. Carneiro, Michael C. Jennings, and Nathan D. Jones Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . methyl 2-[(1R,2R)-2-hydroxy-1,5,5-trimethyl-6-methylenecyclohexyl]acetate C13H22O3 ÏàËÆ¶È:53.8% Indian Journal of Chemistry 2008 47B 449-459 Enantiospecific synthesis of thaps-8-en-5-ol via stereospecific Srikrishna,A; Anebouselvy,K Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . ( +)-Erythro-N-isobutyl-4, 5-dihydroxy-2 (E)-decenamide ÏàËÆ¶È:53.8% Phytochemistry 1983 22 1028-1030 Total synthesis of sylvamide, A Piper alkamide Avijit Banerji, Sudhir C. Pal Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . N,N'-¦Á,¦Á '-di-tert-Boc-(3,3'(1,3-phenylene)diprop-2-yn-1-amide)-amino hexanoic acid C32H42N4O6 ÏàËÆ¶È:53.8% Bioorganic & Medicinal Chemistry 2008 16 3744-3758 Synthesis and evaluation of homodimeric GnRHR antagonists having a rigid bis-propargylated benzene core Kimberly M. Bonger, Richard J.B.H.N. van den Berg, Annemiek D. Knijnenburg, Laura H. Heitman, Ad P. IJzerman, Julia Oosterom, Cornelis M. Timmers, Herman S. Overkleeft, Gijsbert A. van der Marel Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 3,6-bis(6-chlorohexanamido)acridone C25H29N3O3 ÏàËÆ¶È:53.8% Journal of Medicinal Chemistry 2006 49 582-599 Trisubstituted Acridines as G-quadruplex Telomere Targeting Agents. Effects of Extensions of the 3,6- and 9-Side Chains on Quadruplex Binding, Telomerase Activity, and Cell Proliferation Michael J. B. Moore, Christoph M. Schultes, Javier Cuesta, Francisco Cuenca, Mekala Gunaratnam, Farial A. Tanious, W. David Wilson, and Stephen Neidle Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 8-tert-butyl-3-isopropyl-1,4-dioxaspiro[4.5]decan-2-one ÏàËÆ¶È:53.8% Indian Journal of Chemistry 2012 51B 323-327 Iodine catalyzed protection of -hydroxy acids and its application for the synthesis of -hydroxy lactone Sharma, Chinta Mani; Kashyap, Bishwapran; Phukan, Prodeep Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . di-tert-butyl(5'-(tert-butyl)-[1,1':3',1''-terphenyl]-3,3''-diyl)dicarbamate C32H40N2O4 ÏàËÆ¶È:53.8% Tetrahedron 2012 68 6071-6078 Synthesis, structure, and conformation of terphenylene-derived azacalix[4]aromatics Wen-Jing Hu, Ming-Liang Ma, Xiao-Li Zhao, Fang Guo, Xian-Qiang Mi, Biao Jiang, Ke Wen Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . compound 2l C30H34N2O6 ÏàËÆ¶È:53.8% Tetrahedron 2012 68 6914-6919 Visible light induced intermolecular [2+2]-cycloaddition reactions of 3-ylideneoxindoles through energy transfer pathway You-Quan Zou, Shu-Wen Duan, Xiang-Gao Meng, Xiao-Qiang Hu, Shuang Gao, Jia-Rong Chen, Wen-Jing Xiao Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . compound 10 ÏàËÆ¶È:53.8% Australian Journal of Chemistry 1989 42 2071-2084 Norisoprenoids in Vitis vinifera White Wine Grapes and the Identification of a Precursor of Damascenone in These Fruits MA Sefton, GK Skouroumounis, RA Massywestropp and PJ Williams Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . (R)-6-(2,3-dihydroxy-3-methylbutyl)indolin-2-one C13H17NO3 ÏàËÆ¶È:53.8% Magnetic Resonance in Chemistry 2013 51 188-191 Structure elucidation of four prenylindole derivatives from Streptomyces sp. isolated from Ailuropoda melanoleuca feces Dan Zheng, Li Han, Yi Jiang, Yan-Ru Cao, Jiang Liu, Xiu Chen, Yi-Qing Li and Xue-Shi Huang Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-09-30 14:49:19
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ר¼Ò¾Ñé: +726 - PhEPI: 3
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- ¹ó±ö: 0.598
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3Â¥2013-09-30 14:49:42
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