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13C NMR acetone 20.35,23.40,102.22,112.49,116.75,117.82,143.81,161.24,162.22,165.10,179.92 |
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¹û¹û½ÇÂä: ½ð±Ò+20, ¡ïÓаïÖú 2013-07-07 21:50:22
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¹û¹û½ÇÂä: ½ð±Ò+20, ¡ïÓаïÖú 2013-07-07 21:50:22
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°´´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£º¹²²éµ½28¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 7-hydroxy-2,5-dimethyl 4-H-1-benzopyran-4-one C11H10O3 ÏàËÆ¶È:72.7% Natural Product Research and Development 2000 12(2) 1-3 A NEW ALKALOID FROM THE SEEDS OF ALLIUM TUBEROSUM Sang Shengmin; Mao Shilong; Lao Aina; Chen Zhongliang Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . (-)-(1'R,2'S)-erythro-5-hydroxy-7-(1',2'-dihydroxypropyl)-2-methyl-chromone C13H14O5 ÏàËÆ¶È:69.2% Acta Pharmaceutica Sinica 2010 45 1139-1143 A new chromone derivative from Berchemia lineata SHEN Yu-xia, TENG Hong-li, YANG Guang-zhong, MEI Zhi-nan *, CHEN Xiao-long Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 5-hydroxy-7-(2'-hydroxypropyl)-2-methyl-chromone ÏàËÆ¶È:61.5% Acta Pharmaceutica Sinica 2010 45 1139-1143 A new chromone derivative from Berchemia lineata SHEN Yu-xia, TENG Hong-li, YANG Guang-zhong, MEI Zhi-nan *, CHEN Xiao-long Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . mycoleptione C14H16O4 ÏàËÆ¶È:57.1% The Journal of Antibiotics 2012 65 627-629 Mycoleptione, a new chromone derivative isolated from the endophytic fungus Mycoleptodiscus sp. MU41 Ratklao Siriwach, Hiroshi Kinoshita, Shigeru Kitani, Yasuhiro Igarashi, Kanokthip Pansuksan, Watanalai Panbangred and Takuya Nihira Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . compound 9 ÏàËÆ¶È:54.5% Helvetica Chimica Acta 1976 59 903-907 13C-NMR.-Spektren N-acylierter Indoline. Einfluss der Orientierung der Carbonylgruppe auf die chemische Verschiebung Hans Fritz und Tammo Winkler Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . compound 35 ÏàËÆ¶È:54.5% Journal of Heterocyclic Chemistry 2001 38 1409-1418 Synthesis of 7-acetyloxy-3,7-dimethy1-7,8-dihydro-6H-isochromene-6,8-dione and its analogues Tsuneo Suzuki, Kiyoshi Tanemura, Chizuko Okada, The Late Kenichi Arai, Akira Awaji, Takahachi Shimizu and Takaaki Horaguchi Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . Papulasporin C12H12O4 ÏàËÆ¶È:54.5% Chemistry & Biodiversity 2010 7 2941-2950 Chemical Constituents of Papulaspora immersa, an Endophyte from Smallanthus sonchifolius (Asteraceae), and Their Cytotoxic Activity Margareth Borges Coutinho Gallo, Bruno Co¨ºlho Cavalcanti, Francisco Washington Ara¨²jo Barros, Manoel Odorico de Moraes, Let¨ªcia Veras Costa-Lotufo, Cl¨¢udia Pessoa, Jairo Kenupp Bastos and Mônica Tallarico Pupo Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . compound 4a ÏàËÆ¶È:54.5% Archiv der Pharmazie 2006 339 608-615 Novel Synthesis of 1,3,4-Thiadiazine Derivatives and Their Cycloaddition Reactions Wagnat W. Wardakhan Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . (E)-2-cyano-N-cyclopropyl-3-(4-hydroxyphenyl)acrylamide C13H12N2O2 ÏàËÆ¶È:54.5% Bioorganic & Medicinal Chemistry 2011 19 7318-7337 Arylcyanoacrylamides as inhibitors of the Dengue and West Nile virus proteases Christoph Nitsche, Christian Steuer, Christian D. Klein Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . (R)-(-)-5-Chloro-8-hydroxy-3-methyl-1-oxo-3,4-dihydro-(1H)-2-benzopyran-7-carboxylic acid ÏàËÆ¶È:54.5% Australian Journal of Chemistry 2002 55 213-217 Pigments of Fungi. LXIX. Total Synthesis of (R)-Ochratoxin ¦Á and the Formal Total Synthesis of Ochratoxin C. Donner and M. Gill Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 2,5-dimetyl-7-methoxychromone C12H12O3 ÏàËÆ¶È:54.5% Journal of Chinese Medicinal Materials 2005 28 658-660 Studies on Chemical Constituents of Rheum glabricaule Wei Yuhui, Wu Xin¡ä an, Zhang Chengzhong, Li Chong Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . desmethylaltenusin C14H12O6 ÏàËÆ¶È:53.8% Journal of Natural Products 2008 71(6) 972-980 Cytotoxic Metabolites from the Fungal Endophyte Alternaria sp. And Their Subsequent Detection in Its Host Plant Polygonum senegalense Amal H. Aly, RuAngelie Edrada-Ebel, Ine Dewi Indriani, Victor Wray, Werner E. G. Mu#ller, Frank Totzke,Ute Zirrgiebel, Christoph Scha#chtele, Michael H. G. Kubbutat, W. H. Lin, Peter Proksch, and Rainer Ebel Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . isoliquiritigenin ÏàËÆ¶È:53.8% China Journal of Chinese Materia Medica 2008 33 1852-1855 Chemical Constituents from the Caesalpinia millettii CHEN Ping, YANG Junshan Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 5-Amino-2-chloro-6,7,8,9-tetrahydrobenzo[1,8-b]-naphthyridine-3-carbonitrile C13H11ClN4 ÏàËÆ¶È:53.8% Bioorganic & Medicinal Chemistry 2011 19 122-133 Cholinergic and neuroprotective drugs for the treatment of Alzheimer and neuronal vascular diseases. II. Synthesis, biological assessment,and molecular modelling of new tacrine analogues from highly substituted 2-aminopyridine-3-carbonitriles Abdelouahid Samadi, Carolina Valderas, Crist¨®bal de los R¨ªos, Agatha Bastida, Mourad Chioua,Laura Gonz¨¢lez-Lafuente, In¨¦s Colmena, Luis Gand¨ªa, Alejandro Romero, Laura del Barrio,Mar¨ªa D. Mart¨ªn-de-Saavedra, Manuela G. L¨®pez, Mercedes Villarroya, Jos¨¦ Mar Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 3-hydroxy-7,8,9,10-tetrahydro-6H-benzo[c]chromen-6-one C13H12O3 ÏàËÆ¶È:53.8% Heterocycles 2007 71 2721-2733 Al2O3/MeSO3H (AMA) as a Novel Heterogeneous System for Synthesis of Coumarins under Mild Conditions Hashem Sharghi and Mahboubeh Jokar Structure 13C NMR ̼Æ×Ä£Äâͼ |

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