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ÁúÐÄÍõ: ½ð±Ò+8, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-10-15 16:43:41
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ÁúÐÄÍõ: ½ð±Ò+8, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-10-15 16:43:41
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¶ººÅÓÃÓ¢ÎĸñʽµÄ ²éѯ½á¹û£º¹²²éµ½873¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . (E)-1-(2-Hydroxy-5-methoxyphenyl)-3-(3-methoxyphenytyprop-2-en-1-one ÏàËÆ¶È:70.5% Magnetic Resonance in Chemistry 2013 51 364-370 1H and 13C NMR spectral assignments of 2¡ä-hydroxychalcones Yeonjoong Yong, Seunghyun Ahn, Doseok Hwang, Hyuk Yoon, Geunhyeong Jo, Young Hwa Kim, Sang Ho Kim, Dongsoo Koh and Yoongho Lim Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . Compound 4c ÏàËÆ¶È:66.6% Magnetic Resonance in Chemistry 2010 48 738-744 Synthesis and complete assignment of the 1H and 13C NMR signals of new acetamido and aminoflavonoid derivatives (pages 738¨C744) Gilles Casano, Maxime Robin, Pascale Barbier, Vincent Peyrot and Robert Faure Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 5-(3-Ethynylthienyl)-2,2'-bipyridine C16H10N2S ÏàËÆ¶È:64.7% Canadian Journal of Chemistry 2009 87 533-538 Preparation and properties of thienyl and 2,2¡¯-bithienyl substituted cobalt-bis(semiquinone)valence tautomers Thomas J. O¡¯Sullivan, Brandon Djukic, Paul A. Dube, and Martin T. Lemaire Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 7-(1-benzofuran-2-yl)-2,4-diphenyl-2H-oxazolo[3,4-d]pyrid-azine C19H11N3O2 ÏàËÆ¶È:64.7% Journal of Heterocyclic Chemistry 2009 46 680-686 Convenient synthesis of some new pyrazolo[1,5-a]pyrimidine,pyridine,thieno[2,3-b]pyridine,and isoxazolo[3,4-d]pyridazine derivatives containing benzofuran moiety Abdou O. Abdelhamid Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 2-((1E,3E)-4-(4-(dimethylamino)phenyl)buta-1,3-dienyl)-quinazolin-4(3H)-one C20H19N3O ÏàËÆ¶È:64.7% Journal of Heterocyclic Chemistry 2006 43 1057-1063 Convenient synthesis of some 2-substituted 4(3H)-quinazolinone derivatives I. Philipova,G. Dobrikov,K. Krumova and J. Kaneti Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . spiro[1,3-benzodioxan-4-one-2,9'-xanthene] C20H12O4 ÏàËÆ¶È:64.7% Heterocycles 2002 57 143-149 Silver Ion-mediated Desulfurization-Condensation of Thiocarbonyl Compounds Isao Shibuya,* Yasuo Gama, Masao Shimizu, and Midori Goto Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . N-Methylisocystodamine C19H12N4O ÏàËÆ¶È:64.7% Tetrahedron 2011 67 6679-6681 Cell differentiation inducers from a marine sponge Biemna sp. Reiko Ueoka, Yuji Ise, Shigeru Okada, Shigeki Matsunaga Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 2-(3-hydroxybenzylidene)-1-(7-methoxyquinolin-4-yl)hydrazine C17H15N3O2 ÏàËÆ¶È:64.7% Bioorganic & Medicinal Chemistry 2009 17 6063-6072 Development of antitubercular compounds based on a 4-quinolylhydrazone scaffold. Further structure¨Cactivity relationship studies Sandra Gemma, Luisa Savini, Maria Altarelli, Pierangela Tripaldi, Luisa Chiasserini, Salvatore Sanna Coccone, Vinod Kumar, Caterina Camodeca, Giuseppe Campiani, Ettore Novellino, Sandra Clarizio, Giovanni Delogu, Stefania Butini Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 3-(benzothiazol-2'-ylthio)-4-methyl-6-oxo-1-phenyl-1,6-dihydropyridazine-5-carbonitrile C19H12N4OS2 ÏàËÆ¶È:64.7% Journal of Heterocyclic Chemistry 2011 48 241-248 Studies with 2-(acetonylthio)benzothiazole: Novel synthesis of pyridazin-6(1H)-one, pyridazin-6(1H)-imine, and phthalazine derivatives of antimicrobial and antifungal activities Fatima A. Al-Omran and Adel A. El-Khair Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 2-hydroxyxanthone C13H8O3 ÏàËÆ¶È:64.7% Pharmaceutical Biology 2008 46 250-253 A Naturally Occurring Inhibitory Agent from Hypericum sampsonii. with Activity Against Multidrug-Resistant Staphylococcus aureus. Zhi Yong Xiao, Winnie Ka Po Shiu, Yi Han Zeng, Qing Mu, Simon Gibbons Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 2-hydroxyxanthone C13H8O3 ÏàËÆ¶È:64.7% Chinese Traditional and Herbal Drugs 2012 43 230-233 Study on chemical constituents from heartwood of Caesalpinia sappan CAI Chen-qiu; ZHAO Ming-bo; TANG Li; TU Peng-fei Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 3',4'-dihydroxyfurano[4'',5'',6,7]flavone C17H10O5 ÏàËÆ¶È:64.7% Bioorganic & Medicinal Chemistry 2006 14 6820-6826 Isolation and synthesis of analgesic and anti-inflammatory compounds from Ochna squarrosa L. V. Anuradha, Pullela V. Srinivas, R. Ranga Rao, K. Manjulatha, Muralidhar G. Purohit, J. Madhusudana Rao Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . N-(3-methoxy-2-(3-methoxyphenyl)-4-oxo-4H-chro-men-6-yl)acetamide C19H17NO5 ÏàËÆ¶È:63.1% Bioorganic & Medicinal Chemistry 2010 18 6012-6023 Anti-HIV and antiplasmodial activity of original flavonoid derivatives Gilles Casano, Aur¨¦lien Dum¨¨tre, Christophe Pannecouque, S¨¦bastien Hutter, Nadine Azas, Maxime Robin Structure 13C NMR ̼Æ×Ä£Äâͼ |

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