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chenbangjiao: ½ð±Ò+15, ¡ïÓаïÖú 2014-11-18 15:52:24
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chenbangjiao: ½ð±Ò+15, ¡ïÓаïÖú 2014-11-18 15:52:24
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²éѯ½á¹û£º¹²²éµ½515¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . compound 15 C22H19O11P ÏàËÆ¶È:68.1% Chinese Chemical Letters 2014 25 1044-1046 Synthesis and cytotoxicity evaluation of a novel justicidin G analogue and its phosphate ester Sheng-Peng Wang, Yuan-Feng Tong, Dong-Mei Wang, Nan Wang, Zheng Yan, Ping Huang, Song Wu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . r-1-Phenyl-t-2-benzoyl-c-3-(3,4-methylenedioxyphenyl)-5,6-dimethoxyindane ÏàËÆ¶È:63.6% Tetrahedron 2012 68 913-921 Scope of the formal [3+2] cycloaddition for the synthesis of five-membered ring of functionalized indanes Beatriz Lantaño, Jose Manuel Aguirre, Esteban Ariel Ugliarolo, Rosario Torviso, Nicol¨¢s Pomilio, Graciela Yolanda Moltrasio Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 7-(1-(tert-Butylcarbamoyl)-3,4-dihydroisoquino-lin-2(1H)-yl)-1-cyclopropyl-1,4-dihydro-6-fluoro-8-methoxy-4-oxoquinoline-3-carboxylic acid C28H30FN3O5 ÏàËÆ¶È:60.8% Bioorganic & Medicinal Chemistry 2008 16 2558-2569 Synthesis and antimycobacterial evaluation of newer 1-cyclopropyl-1,4-dihydro-6-fluoro-7-(substituted secondary amino)-8-methoxy-5-(sub)-4-oxoquinoline-3-carboxylic acids Palaniappan Senthilkumar, Murugesan Dinakaran, Debjani Banerjee, Ruth Vandana Devakaram, Perumal Yogeeswari, Arnab China, Valakunja Nagaraja, Dharmarajan Sriram Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . (2S)-5,7-dimethoxy-8-(2S-hydroxy-3-methyl-3-butenyl)flavanone C22H24O5 ÏàËÆ¶È:59.0% Journal of Natural Products 2003 66 1197-1202 Constituents of the Stem Bark of Pongamia pinnata with the Potential to Induce Quinone Reductase Esperanza J. Carcache-Blanco,Young-Hwa Kang,Eun Jung Park,Bao-Ning Su, Leonardus B. S. Kardono,Soedarsono Riswan, Harry H. S. Fong, John M. Pezzuto, and A. Douglas Kinghorn Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . (-)-(2R,3R)-5,7-dimethoxy-3',4'-methylenedioxy-flavan-3-ol ÏàËÆ¶È:59.0% Natural Product Research 2006 20 1199-1206 Chemical constituents from Phoebe minutiflora II Yuan-Ling Ku; Chung-Hsiung Chen; Shoei-Sheng Lee Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . diphyllin ÏàËÆ¶È:59.0% Phytochemistry 1994 35 1600-1601 An alkaloid and lignans from Haplophyllum telephioides A. Ulubelen, A.H. Meriçli, F. Meriçli, ¨¹ Kaya Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 3-(4-hydroxy-3-methoxyphenyl)-3,3a,4,5-tetrahydronaphth-[1,2-c]isoxazole C18H17NO3 ÏàËÆ¶È:59.0% Journal of Heterocyclic Chemistry 2006 43 315-319 Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 1-benzyl-7,8-dimethoxy-3-phenylpyrazolo[5,4-c]isoquinoline C25H21N3O2 ÏàËÆ¶È:59.0% Journal of Heterocyclic Chemistry 2001 38 523-525 Convenient one pot synthesis of 5-unsubstituted pyrazolo [3,4-c]isoquinolines Sergei L. Bogza, Anna A. Malienko, Sergei Y U. Sujkov, Igor F. Perepichka, Natalya M. Bogdan, Vladimir I. Dulenko, Konstantin I. Kobrakov and Martin R. Bryce Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . 3-phenylazo-5,6-dihydro-8,9-dimethoxy-2-phenylpyrrolo[2,1-a]isoquinoline C26H23N3O2 ÏàËÆ¶È:59.0% Heterocycles 2008 75 2779-2789 A Facile Route to Pyrrolo[2, 1-a]- and 1, 2, 3-Triazolo[5, 1-a]dihydroisoquinolines Tayseer A. Abdallah Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . compound 2a C24H25NO4S2 ÏàËÆ¶È:59.0% Tetrahedron Letters 2003 44 6137-6140 Thioorthoesters in the activated Pictet¨CSpengler cyclization. Synthesis of 1-thiosubstituted tetrahydroisoquinolines and carbon---carbon bond formation via sulfonyl iminium ions generated from N,S-sulfonyl acetals Claudio C Silveira, Carmem R Bernardi, Antonio L Braga, Teodoro S Kaufman Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . ethyl (6R,7S,8R,9R)-7-cinnamyl-5,7,8,9-tetrahydro-6,9-methano-[1,3]dioxolo[4',5':4,5]benzo[1,2-c]azepine-8-carboxylate C24H25NO4 ÏàËÆ¶È:59.0% European Journal of Organic Chemistry 2011 4571-4587 One-Step Stereospecific Strategy for the Construction of the Core Structure of the 5,11-Methanomorphanthridine Alkaloids in Racemic as well as in Optically Pure Form: Synthesis of (¡À)-Pancracine and (¡À)-Brunsvigine Ganesh Pandey, Ravindra Kumar, Prabal Banerjee and Vedavati G. Puranik Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . (1R,2R,3S,4S,5S,6S)-3,4-dihydroxy-5,6-(isopropylidenedioxy)-2-(3',4'-methylenedioxyphenylmethyl)-1-cyclohexyl-benzenesulfonamide C31H35NO9S ÏàËÆ¶È:59.0% Canadian Journal of Chemistry 2001 79 1659-1667 Structure assignment of aminoconduritols by 15N NMR correlation spectroscopy; synthesis of a positional isomer of 7-deoxypancratistatin Stefan Schilling, Uwe Rinner, Collin Chan, Ion Ghiviriga, Tomas Hudlicky Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . (Z)-2-(benzo[d][1,3]dioxol-5-ylmethyl)-3-benzylideneisoindolin-1-one C23H17NO3 ÏàËÆ¶È:59.0% Molecules 2013 18 654-665 Efficient Synthesis of a (Z)-3-Methyleneisoindolin-1-one Library Using Cu(OAc)2•H2O/DBU under Microwave Irradiation Li Zhang, Yongliang Zhang, Xin Wang and Jingkang Shen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . compound 1 ÏàËÆ¶È:59.0% Magnetic Resonance in Chemistry 1993 31 868-875 13C NMR data for several cyclolignans A. San Feliciano, J. M. Miguel Del Corral, M. Gordaliza and M. A. Castro Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . 1-Methylapocodeine C19H21NO2 ÏàËÆ¶È:59.0% Bioorganic & Medicinal Chemistry 2013 21 4143-4150 1-substituted apomorphines as potent dopamine agonists Reet Reinart-Okugbeni, Argo Vonk, Ain Uustare, Zsuzsanna Gyulai, Attila Sipos, Ago Rinken Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . (2R,3R)-3-hydroxy-5,7-dimethoxy-3',4'-methylenedioxy-flavan C18H18O6 ÏàËÆ¶È:59.0% Journal of Central China Normal University (Nature Science) 2012 46 695-699,724 Phenols from the stem of Machilus ichangensis Rehd. et Wils. Cheng Fan, Xu Bang, Guo Lingzhi, Guo Zhiyong, Zou Kun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . N-Phenylpyrazole curcumin ÏàËÆ¶È:58.3% Bioorganic & Medicinal Chemistry 2008 16 2894-2902 Synthesis and exploration of novel curcumin analogues as anti-malarial agents Satyendra Mishra, Krishanpal Karmodiya, Namita Surolia, Avadhesha Surolia Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . 4'-demethoxy-3',4'-methylenedioxyrocaglaol C26H24O7 ÏàËÆ¶È:58.3% Tetrahedron 1997 53 17625-17632 Novel cytotoxic 1H-cyclopentabenzofuran lignans from Aglaia elliptica Baoliang Cui, Heebyung Chai, Thawatchai Santisuk, Vichai Reutrakul, Norman R. Farnsworth, Geoffrey A. Cordell, John M. Pezzuto, A. Douglas Kinghorn Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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