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13C NMR (101 MHz, CDCl3) 14.7 ,60.5 ,77.4 ,77.8 ,83.4 ,115.9 ,124.3 ,126.3 ,127.1 ,127.8 ,131.3 ,134.6 ,134.9 ,139.3 ,147.7 ,161.2 ,171.7 |
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²éѯ½á¹û£º¹²²éµ½234¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . (-)-chaetominine ÏàËÆ¶È:71.4% Chinese Pharmaceutical Journal 2011 46 1154-1158 Metabolites of Aspergillus sp. HT-2 ZHANG, Li-min, LI, Zhan-lina, BAI, Jiao, Wu, Xinc, WANG, Yu, HUA, Hui-ming Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . Ethyl 2-(4-oxo-2-thioxo-1,2-dihydroquinazolin-3(4H)-yl)benzoate C17H14N2O3S ÏàËÆ¶È:64.7% Zeitschrift f¨¹r Naturforschung B 2009 64 1065-1069 Synthesis and Single Crystal X-Ray Structure of Bis[4-oxo-3-(2-ethoxycarbonylphenyl)-3,4-dihydroquinazolin-2-yl]disulfide M. Rimaz, J. Khalafy, K. Tavana, K. \'Slepokura, T. Lis, A. Souldozi, A. T. Mahyari, N. Shajari, and A. Ramazani Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . Bis[4-oxo-3-(2-ethoxycarbonylphenyl)-3,4-dihydroquinazolin-2-yl]disulfide C34H26N4O6S2 ÏàËÆ¶È:64.7% Zeitschrift f¨¹r Naturforschung B 2009 64 1065-1069 Synthesis and Single Crystal X-Ray Structure of Bis[4-oxo-3-(2-ethoxycarbonylphenyl)-3,4-dihydroquinazolin-2-yl]disulfide M. Rimaz, J. Khalafy, K. Tavana, K. \'Slepokura, T. Lis, A. Souldozi, A. T. Mahyari, N. Shajari, and A. Ramazani Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . Chaetominine C22H18N4O4 ÏàËÆ¶È:63.6% Organic Letters 2006 8 5709-5712 Chaetominine, a Cytotoxic Alkaloid Produced by Endophytic Chaetomium sp. IFB-E015 Rui H. Jiao, Shu Xu,Jun Y. Liu, Hui M. Ge, Hui Ding, Chen Xu, Hai L. Zhu, and Ren X. Tan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . Ethyl 2-benzoyl-4-ethoxy-5-oxo-2-phenyl-2,5-dihydro-3-furancarboxylate C22H20O6 ÏàËÆ¶È:61.1% Chinese Chemical Letters 2011 22 49-52 Efficient synthesis of functionalized butenolides mediated by vinyltriphenylphosphonium salts in aqueous media Mohammad A. Khalilzadeh, Adel Hasannia, Mohammad M. Baradarani, Zinatossadat Hossaini Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . Tryptoquivaline J C22H18N4O4 ÏàËÆ¶È:59.0% Chemistry of Natural Compounds 2005 41 236-238 ALKALOIDS FROM THE MARINE ISOLATE OF THE FUNGUS Aspergillus fumigatus Sh. Sh. Afiyatullov, A. I. Kalinovskii, M. V. Pivkin,P. S. Dmitrenok, and T. A. Kuznetsova Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . ethyl 5-hydroxy-7-naphthalen-1-ylindane-4-carboxylate C22H20O3 ÏàËÆ¶È:59.0% Chemical & Pharmaceutical Bulletin 2013 61 768¨C775 One-Pot Synthesis of Phenol Derivatives by the Novel Intramolecular Alder¨CRickert Reaction: Effects of Aryl Substituent at the 3-Position of Cyclohexenone Derivatives on Reactivity Atsushi Kinbara, Takehiro Yamagishi, Takeshi Fujishige, Hiroaki Miyaoka Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . trans-3,5-Dimethoxystilben-4'-O-¦Â-D-glucopyranoside C22H26O8 ÏàËÆ¶È:58.8% Chemistry of Natural Compounds 2012 48 1-7 REACTION OF SEVERAL RESVERATROL GLYCOSIDE DERIVATIVES WITH HYPOCHLORITES IN VARIOUS MEDIA A. D. Rogachev,N. I. Komarova,A. V. Pozdeeva,D. V. Korchagina,V. G. Vasil ev,N. F. Salakhutdinov,and G. A. Tolstikov1 Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . Compound 3 ÏàËÆ¶È:58.8% Magnetic Resonance in Chemistry 2000 38 386-387 13C NMR spectral characterization of N-aryl-substituted 4H-1, 4-benzothiazine 1, 1-dioxide |
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