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²éѯ½á¹û£º¹²²éµ½131¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . compound G. C48H57NO7SSi ÏàËÆ¶È:60.6% Tetrahedron 2013 69 4120-4138 Novel method for construction of tetrahydro-1-benzazepine and tetrahydro-2-benzazepine based on 7-endo selective Friedel¨CCrafts cyclization of vinyloxirane Megumi Mizukami, Koji Wada, Gen Sato, Yusuke Ishii, Norio Kawahara, Shinji Nagumo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . (1S,4aS,8aR)-Methyl-5-{2-[2-(2-oxo-2-benzylaminoacetyl)furan-3-yl]ethyl}-1,4a,6-trimethyl-1,2,3,4,4a,7,8,8aoctahydronaphthalen- 1-carboxylate C30H37NO5 ÏàËÆ¶È:56.6% Chemistry of Natural Compounds 2010 46 233-241 Synthetic transformations of higher terpenoids. XXI.* Preparation of phlomisoic acid and its N-containing derivatives M. E. Mironov, Yu. V. Kharitonov, E. E. Shul¡¯ts, M. M. Shakirov and I. Yu. Bagryanskaya, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . sarcotragins A C31H43NO4 ÏàËÆ¶È:56.6% Tetrahedron Letters 2001 42 3005-3007 Sarcotragins A and B, new sesterterpenoid alkaloids from the sponge Sarcotragus sp. Jongheon Shin, Jung-Rae Rho, Youngwan Seo, Hyi-Seung Lee, Ki Woong Cho, Chung J. Sim Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 2-[N-(tolylsulfonyl)-N-[4-[(tert-butyldiphenylsilyl)oxy]butyl]amino]-4-[(tert-butyldiphenylsilyl)oxy]-1-iodo-butan-4-ol C47H60INO4SSi2 ÏàËÆ¶È:56.6% Journal of Medicinal Chemistry 1995 38 2714-2727 Synthesis and Biochemical Evaluation of Adenosylspermidine, a Nucleoside-Polyamine Adduct Inhibitor of Spermidine Synthase John R. Lakanen, Anthony E. Pegg, James K. Coward Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . N-(tert-butyl)-9-{4-[4-(tert-butyldiphenylsilyloxy)-methyl]benzoylphenyl}-3,4-dihydro-2H,6H-pyrimido[1,2-c][1,3]benzothiazin-6-imine C45H47N3O2SSi ÏàËÆ¶È:56.6% Bioorganic & Medicinal Chemistry 2013 21 2079-2087 Design and synthesis of biotin- or alkyne-conjugated photoaffinity probes for studying the target molecules of PD 404182 Tsukasa Mizuhara, Shinya Oishi, Hiroaki Ohno, Kazuya Shimura, Masao Matsuoka, Nobutaka Fujii Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . Mesylate C28H36O4S ÏàËÆ¶È:56.6% Journal of the American Chemical Society 1998 120 12777-12782 A Direct and Efficient Stereocontrolled Synthetic Route to the Pseudopterosins, Potent Marine Antiinflammatory Agents E. J. Corey and Scott E. Lazerwith Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . 9-((1R,3R,4R,7S)-7-(Benzyloxy)-1-((tert-butyldiphenylsilyloxy) methyl)-2,5-dioxabicyclo[2.2.1]heptan-3-yl)-2,6-di(furan-2-yl)-9H-purine C42H40N4O6Si ÏàËÆ¶È:56.2% Bioorganic & Medicinal Chemistry 2011 19 5648-5669 Synthesis and biological evaluation of 2', 4'- and 3', 4'-bridged nucleoside analogues K.C. Nicolaou, Shelby P. Ellery, Fatima Rivas, Karen Saye, Eric Rogers, Tyler J. Workinger, Mark Schallenberger, Rommel Tawatao, Ana Montero, Ann Hessell, Floyd Romesberg, Dennis Carson, Dennis Burton Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . 1-(4-chlorophenyl)-3,3-bis(4-methylphenyl)-1'-methyl-spiro-[azetidine-2,3'-indoline]-2',4-dione C31H25N2O2Cl ÏàËÆ¶È:53.3% Journal of Heterocyclic Chemistry 2006 43 1665-1668 Reactions of ¦Á-diazoketones with indolinone imines: Synthesis of new 1,3,3-triaryl-1'-methylspiro[azetidine-2,3'-indoline]-2',4-diones Girija S. Singh and Boycie J. Mmolotsi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . compound 26c C31H29N3O6 ÏàËÆ¶È:53.3% Heterocycles 2006 70 367-388 Cycloaddition Reactions of Amino-Acid Derived Cross-Conjugated Trienes: Stereoselective Synthesis of Novel Heterocyclic Scaffolds Branko Mitasev, Bingli Yan, and Kay M. Brummond* Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . Jolkinol B C29H36O5 ÏàËÆ¶È:53.3% Chinese Traditional and Herbal Drugs 2004 35 611-613 Diterpenoids from Euphorbia wallichii WANG Huan; ZHANG Xiao-feng; MA Yun-bao; CAI Xiang-hai; WU Da-gang; LUO Xiao-dong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . 3,8-Dimethyl-N,N,5-tri(propan-2-yl)benzoheptaleno[1',2':5,6]benzo[1,2-d]thiophen-10-amine 11,11-dioxide C33H37NO2S ÏàËÆ¶È:53.3% Heterocycles 2011 82 1195-1202 Nucleophilic Reactions of 9-Isopropyl-2,4-dimethoxy-7,12-dimethyl-3-(phenylsulfonyl)benzo[a]heptalene with Lithium Dialkylamides Samir El Rayes, Anthony Linden, Khaled Abou-Hadeed, and Hans-J¨¹rgen Hansen* Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . syn-(¡À)-4-(2'-Methoxybiphenyl-4-yl)-3,6-dimethyl-1-(2-methylphenyl)-4,8-dihydro-1H-pyrazole[3,4-e][1,4]thiazepin-7-one C28H27N3OS ÏàËÆ¶È:53.3% Bioorganic & Medicinal Chemistry 2012 20 3429-3445 Pyrazole[3,4-e][1,4]thiazepin-7-one derivatives as a novel class of Farnesoid X Receptor (FXR) agonists Maura Marinozzi, Andrea Carotti, Emanuele Sansone, Antonio Macchiarulo, Emiliano Rosatelli, Roccaldo Sardella, Benedetto Natalini, Giovanni Rizzo, Luciano Adorini, Daniela Passeri, Francesca De Franco, Mark Pruzanski, Roberto Pellicciari Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . (4-Benzyloxy-3-isopropylphenyl)-(7-dibenzylamino-5-methylindan-4-yl)methanol C41H43NO2 ÏàËÆ¶È:53.3% Bioorganic & Medicinal Chemistry 2012 20 3622-3634 Discovery of novel indane derivatives as liver-selective thyroid hormone receptor ¦Â (TR¦Â) agonists for the treatment of dyslipidemia Hiroaki Shiohara, Tetsuya Nakamura, Norihiko Kikuchi, Tomonaga Ozawa, Ryuichi Nagano, Akane Matsuzawa, Hideki Ohnota, Takahide Miyamoto, Kazuo Ichikawa, Kiyoshi Hashizume Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . [(2S,3S)-3-{(E,3R,4R,5R,6R)-5-[(tert-Butyldimethylsilyl)oxy]-7-[(tert-butyldiphenylsilyl)oxy]-3-methoxy-1,4,6-trimethyl-1-heptenyl}-oxiran-2-yl]methyl 4-Methyl-1-benzenesulfonate C43H64O7Si2S ÏàËÆ¶È:53.3% European Journal of Organic Chemistry 2012 2062-2071 Towards the Synthesis of (¨C)-Callipeltoside A: Stereoselective Synthesis of the C1¨CC14 Macrolactone Core Jhillu S. Yadav, Animesh Haldar and Tapas Maity Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . (2R,4E,6R,7R,8R,9R)-8-[(tert-Butyldimethylsilyl)oxy]-10-[(tert-butyldiphenylsilyl)oxy]-2-hydroxy-6-methoxy-4,7,9-trimethyl-4-decenyl-4-Methyl-1-benzenesulfonate C43H66O7Si2S ÏàËÆ¶È:53.3% European Journal of Organic Chemistry 2012 2062-2071 Towards the Synthesis of (¨C)-Callipeltoside A: Stereoselective Synthesis of the C1¨CC14 Macrolactone Core Jhillu S. Yadav, Animesh Haldar and Tapas Maity Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . Z,E,Z-cupaniopsin C 22-hydroxy derivative C30H44O4 ÏàËÆ¶È:53.3% Tetrahedron 2005 61 845-851 New biologically active linear triterpenes from the bark of three new-caledonian Cupaniopsis species H. Bousserouel, M. Litaudon, B. Morleo, M.-T. Martin, O. Thoison, O. Nosjean, J.A. Boutin, P. Renard, T. S¨¦venet Structure 13C NMR ̼Æ×Ä£Äâͼ |
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