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| 13C NMR(CD3OD) 30.6,49.6,55.8,56.0,56.9,64.8,112.7,116.3,121.8,125.4,129.6,146.8,148.9,199.0 |
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ÓÍÌï±ø¶¡: ½ð±Ò+8, ¡ïÓаïÖú 2015-05-09 15:57:17
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²éѯ½á¹û£º¹²²éµ½139¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . (-)-evofolin B C17H18O6 ÏàËÆ¶È:75% Chemistry of Natural Compounds 2013 49 486-492 Chemical Constituents from Aphanamixis grandifolia Qi Zeng, Ji Ye, Jie Ren, Xiang-rong Cheng, Jiang-jiang Qin, Hui-Zi Jin, Wei-Dong Zhang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . Evofolin-B C17H18O6 ÏàËÆ¶È:73.3% Phytochemistry 1995 40 121-124 The heartwood constituents of Tetradium glabrifolium Tian-Shung Wu, Jyh-Her Yeh, Pei-Lin Wu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . [(1R,3S)-6,7-dimethoxy-1-phenyl-1,2,3,4-tetrahydroisoquinolin-3-yl]methanol C28H21NO3 ÏàËÆ¶È:73.3% European Journal of Organic Chemistry 2010 972-980 Synthesis and Screening of C1-Substituted Tetrahydroisoquinoline Derivatives for Asymmetric Transfer Hydrogenation Reactions Sai Kumar Chakka, Pher G. Andersson, Glenn E. M. Maguire, Hendrik G. Kruger and Thavendran Govender Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . (R)-Calycotomine C12H17NO3 ÏàËÆ¶È:71.4% Molecules 2004 9 650-657 Isolation and X-ray Crystal Structure of Tetrahydroisoquinoline Alkaloids from Calycotome Villosa Subsp. Intermedias Ali El Antri, Ibtissam Messouri, Mohamed Bouktaib, Rachid El Alami, Michael Bolte, Brahim El Bali and Mohammed Lachkar Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 4'-O-Methylnorbelladine ÏàËÆ¶È:71.4% Phytochemistry 1998 49 1037-1047 Biosynthesis of the amaryllidaceae alkaloid Galanthamine Jörg Eichhorn, Takeshi Takad¦Á, Yasuyuki Kit¦Á, Meinhart H. Zenk Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . (+)-crispine A C14H19NO2 ÏàËÆ¶È:71.4% The Journal of Organic Chemistry 2011 76 1605-1613 Concise Enantiospecific, Stereoselective Syntheses of (+)-Crispine A and Its (-)-Antipode Mahender Gurram,Bal azs Gyim othy, Ruifang Wang, Sang Q. Lam, Feryan Ahmed, and R. Jason Herr Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . (R)-Crispine A C14H20NO2 ÏàËÆ¶È:71.4% Tetrahedron 2011 67 8648-8653 Stereoselective synthesis of tetrahydroisoquinoline alkaloids: (-)-trolline,(+)-crispin A, (+)-oleracein E Nobuyuki Kawai , Mika Matsuda, Jun¡¯ichi Uenishi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . (¡À)-Crispine A ÏàËÆ¶È:71.4% Tetrahedron Letters 2005 46 1173-1175 Total synthesis of the antitumor active pyrrolo[2,1-a]isoquinoline alkaloid (¡À)-crispine A Hans-Joachim Knölker, Sameer Agarwal Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . Crispine A ÏàËÆ¶È:71.4% Tetrahedron 2002 58 6795-6798 Novel bioactive isoquinoline alkaloids from Carduus crispus Qingying Zhang, Guangzhong Tu, Yuying Zhao, Tieming Cheng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . (S)-(-)-crispine A C14H19NO2 ÏàËÆ¶È:71.4% European Journal of Organic Chemistry 2010 4017-4026 A General Methodology for the Enantioselective Synthesis of 1-Substituted Tetrahydroisoquinoline Alkaloids Mercedes Amat, Viviane Elias, N¨²ria Llor, Fabiana Subrizi, Elies Molins and Joan Bosch Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . dubiamine C18H21NO3 ÏàËÆ¶È:71.4% Journal of Ethnopharmacology 2012 143 310-313 Antimalarial alkaloids from a Bhutanese traditional medicinal plant Corydalis dubia Phurpa Wangchuk, Paul A. Keller, Stephen G. Pyne, Anthony C. Willis, Sumalee Kamchonwongpaisan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . compound 10 ÏàËÆ¶È:71.4% Magnetic Resonance in Chemistry 1987 25 423-428 Dimethoxy aromatic compounds. IV.¡ªdetermination of stereochemistry of 2,3,6,7-tetraalkoxy-9,10-dihalomethyl-9,10-dihydroanthracenes by 13C NMR chemical shifts Liliana Lamartina, Leopoldo Ceraulo and Maria C. Natoli Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . compound 12 ÏàËÆ¶È:71.4% Magnetic Resonance in Chemistry 1987 25 423-428 Dimethoxy aromatic compounds. IV.¡ªdetermination of stereochemistry of 2,3,6,7-tetraalkoxy-9,10-dihalomethyl-9,10-dihydroanthracenes by 13C NMR chemical shifts Liliana Lamartina, Leopoldo Ceraulo and Maria C. Natoli Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . evofolin-B ÏàËÆ¶È:70.5% Chinese Pharmaceutical Journal 2008 43 1066-1069 Studies on Chemical Constituents in Fruit of Melia toosendan XIE Fan, ZHANG mian, ZHANG Chao-feng, WANG Zheng-tao, YU Bo-yang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . evofolin B C17H18O6 ÏàËÆ¶È:70.5% Chinese Journal of Medicinal Chemistry 2009 19 55-58 Chemical constituents of Paeonia albiflora DUAN Wen-juan, JIANG Yan, JIN Xin, QIN Geng-yao, QIU Feng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . 2-(4-Hydroxy-3-methoxyphenyl)-3-(2-hydroxy-5-methoxyphenyl)-3-oxo-1-propanol C17H18O6 ÏàËÆ¶È:70.5% Bulletin of the Korean Chemical Society 2007 28 1261-1264 Isoetin 5'-Methyl Ether, A Cytotoxic Flavone from Trichosanthes kirilowii Md. Aziz Abdur Rahman, Surk-Sik Moon* Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . (¡À)-evofolin B ÏàËÆ¶È:70.5% Chinese Journal of New Drugs 2011 20 1569-1572 Chemical constituents of Saussurea deltoidea HUANG Huo-qiang, PIAO Xiang-lan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . evofolin B C17H18O6 ÏàËÆ¶È:70.5% Chinese Joumal of Experimental Traditional Medical Fomulae 2012 18 128-130 Studies on Chemical Constituents of Chloroform Portion of Incarvillea arguta MO Xiao-yu, MAI Jing-biao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . (+) Evofolin B C17H18O6 ÏàËÆ¶È:68.7% Acta Botanica Yunnanica 2001 23(3) 368-372 Chemical Constituents from Dysoxylum hainanense LUO Xiao-Dong,WU Shao-Hua,MA Yun-Bao,WU Da-Gang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . evofolin B ÏàËÆ¶È:68.7% China Journal of Chinese Materia Medica 2010 35 1261-1271 Chemical constituents of stems and branches of Adina polycephala ZHANG Yanling; GAN Maoluo; LI Shuai; WANG Sujuan; ZHU Chenggen; YANG Yongchun; HU Jinfeng; CHEN Naihong; SHI Jiangong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 21 . evofolin B ÏàËÆ¶È:68.7% Chinese Traditional and Herbal Drugs 2010 41 539-541 ɽʯÁñµÄ»¯Ñ§³É·ÖÑо¿(¢ò) ¸ß¹ã´º;ÌÕÊïºì;ÆáÊ绪;ÕÅ‚Æ;ÀîÇìÐÀ Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 22 . evofolin-B ÏàËÆ¶È:68.7% Chinese Traditional and Herbal Drugs 2011 42 2394-2397 Chemical constituents from seeds of Hydnocarpus anthelminthica WANG, Jun-feng, YANG, Yang, ZHONG, Hui-min, CHENG, Yong-xian Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 23 . evofolin-B ÏàËÆ¶È:68.7% China Journal of Chinese Materia Medica 2013 38 1172-1182 Chemical consitituents from root of Isatis indigotica WANG Xiao-liang, CHEN Ming-hua, WANG Fang, BU Peng-bin, LIN Sheng, ZHU Cheng-gen, LI Yu-huan, JIANG Jian-dong, SHI Jian-gong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 24 . evofolin B C17H18O6 ÏàËÆ¶È:68.7% Chinese Traditional and Herbal Drugs 2013 44 2358-2363 Chemical constituents from barks of Cinnamomum cassia growing in China ZHAO Kai, YIANG Yong, XUE Pei-feng, TU Peng-fei Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 25 . evofolin B C17H18O6 ÏàËÆ¶È:68.7% Bulletin of the Academy of Military Medical Sciences 2013 37 130-134 Phenylpropanoids from Solanum surattense LI Jie-hui, YIN Hai-long, DONG Jun-xing Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 26 . 4'-O-Methyl-N-methylnorbelladine ÏàËÆ¶È:66.6% Phytochemistry 1998 49 1037-1047 Biosynthesis of the amaryllidaceae alkaloid Galanthamine Jörg Eichhorn, Takeshi Takad¦Á, Yasuyuki Kit¦Á, Meinhart H. Zenk Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 27 . Isocernumidine C15H20N4O3 ÏàËÆ¶È:66.6% Tetrahedron Letters 2011 52 6392-6395 Cernumidine and isocernumidine, new type of cyclic guanidine alkaloids from Solanum cernuum Luciane C. Lopes, Bianca Roman,Maria A. Medeiros ,Abhik Mukhopadhyay , Pilar Utrilla ,Julio G¨¢lvez, Sof¨ªa Garc¨ªa Mauriño , Virginia Moltiva ,Ana Lourenço ,Arturo San Feliciano Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 28 . Compound 3j C17H14N6O ÏàËÆ¶È:66.6% Bioorganic & Medicinal Chemistry Letters 2009 19 5569-5572 Solvent free synthesis of 1,5-disubstituted tetrazoles derived from Baylis Hillman acetates as potential TNF-¦Á inhibitors P. Srihari, Palash Dutta, R. Srinivasa Rao, J.S. Yadav, S. Chandrasekhar, P. Thombare, J. Mohapatra, A. Chatterjee, Mukul R. Jain Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 29 . 2-benzyl-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline C18H21NO2 ÏàËÆ¶È:66.6% European Journal of Organic Chemistry 2011 547-552 Modified B-Alkylcatecholboranes as Radical Precursors Monique L¨¹thy, Vincent Darmency and Philippe Renaud Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 30 . evofolin B C17H18O6 ÏàËÆ¶È:66.6% Military Medical Sciences 2013 37 130-134 Phenylpropanoids from Solanum surattense LI Jie-hui, YIN Hai-long, DONG Jun-xing Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 31 . Methyl 4-morpholinyl-6-(3-hydroxy-4-methoxyphenyl)-2-thioxohexahydropyrimidine-5-carboxylate C17H23N3O5S ÏàËÆ¶È:66.6% Chinese Journal of Chemistry 2014 32 172−178 Diastereoselective Synthesis of Functionalized Tetrahydropyrimidin-2-thiones via ZnCl2 Promoted One-pot Reactions Zhenming Liu, Lili Zhang, Jing Sun, and Chaoguo Yan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 32 . evafolin B |

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