| ²é¿´: 288 | »Ø¸´: 1 | ||
lyy5563Òø³æ (³õÈëÎÄ̳)
|
[ÇóÖú]
΢Æ×ÇóÖú ÒÑÓÐ1È˲ÎÓë
|
| DMSO-d6 184.4,167.4,165.0,160.2,156.9,150.6,143.8,137.8,132.2,132.0,129.1,127.1,114.0,101.7,94.9,71.6,65.5 |
» ²ÂÄãϲ»¶
±¾¿Æ211£¬293·ÖÇëÇóµ÷¼Á
ÒѾÓÐ6È˻ظ´
085600²ÄÁÏÓ뻯¹¤µ÷¼Á
ÒѾÓÐ25È˻ظ´
±¾9Ò»Ö¾Ô¸2 0854µÍ·Öר˶286Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
085600£¬320·ÖÇóµ÷¼Á
ÒѾÓÐ9È˻ظ´
316Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
0856µ÷¼Á
ÒѾÓÐ8È˻ظ´
278Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
0703Çóµ÷¼Á383·Ö
ÒѾÓÐ3È˻ظ´
400·ÖÇóµ÷¼Á
ÒѾÓÐ3È˻ظ´
085701Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
seuseasoar
ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)
- Ó¦Öú: 2238 (½²Ê¦)
- ½ð±Ò: 48394.9
- ºì»¨: 52
- Ìû×Ó: 6742
- ÔÚÏß: 546.4Сʱ
- ³æºÅ: 2400995
- ×¢²á: 2013-04-01
- ÐÔ±ð: MM
- רҵ: ʳƷ¿ÆÑ§»ù´¡
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
lyy5563(׿Խ_ÏÈ·æ´ú·¢): ½ð±Ò+5, ok 2015-05-05 18:40:16
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
lyy5563(׿Խ_ÏÈ·æ´ú·¢): ½ð±Ò+5, ok 2015-05-05 18:40:16
|
1 . eucomin ÏàËÆ¶È:56.2% Chemical & Pharmaceutical Bulletin 2007 55(4) 655-657 Flavonol Galactoside Caffeiate Ester and Homoisoflavones from Caesalpinia millettii HOOK. et ARN. Ping CHEN and Jun-Shan YANG Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . (E)-ethyl 2-(4-amino-1-(4-chlorophenyl)-1H-pyrazolo[3,4-d]pyrimidin-6(7H)-ylidene)-3-oxopropanoate C16H14ClN5O3 ÏàËÆ¶È:56.2% Archiv der Pharmazie 2011 11 184-196 Synthesis and Biological Evaluation of Some Novel Fused Pyrazolopyrimidines as Potential Anticancer and Antimicrobial Agents Heba A. Abd El Razik and Abeer E. Abdel Wahab Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 3-chloro-1-p-methylphenyl-5-oxa-1-azaspiro[3.4]oct-7'-ene-2,6-dione C13H10NO3Cl ÏàËÆ¶È:56.2% Heterocycles 2007 71 531-542 Diastereoselective Synthesis of Spiro-¦Â-lactams via Staudinger Reaction Susana Rojas-Lima, Lidia Santill¨¢n-Sid, Heraclio L¨®pez-Ruiz, and Alejandro ¨¢lvarez-Hern¨¢ndez Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . dioscorone A ÏàËÆ¶È:56.2% Pharmazie 2003 58 214-215 Two new non-steroidal constituents from Dioscorea futschauensis R. Kunth H. W. Liu - S. L. Wang - B. Cai - X. S. Yao Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 2',6'-dichloroflavone ÏàËÆ¶È:56.2% Tetrahedron Letters 2005 46 253-256 Silica gel supported InBr3 and InCl3: new catalysts for the facile and rapid oxidation of 2'-hydroxychalcones and flavanones to their corresponding flavones under solvent free conditions Naseem Ahmed, Hasrat Ali, Johan E. van Lier Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . diethyl {2-[N-(4-amino-1H-pyrimidin-2-on-1-ylmethyl)-N-(p-toluenesulfonyl)amino]ethoxymethyl}phosphonate C19H29N4O7PS ÏàËÆ¶È:56.2% Bioorganic & Medicinal Chemistry 2009 17 3756-3762 Synthesis and antiviral activity evaluation of acyclic 2'-azanucleosides bearing a phosphonomethoxy function in the side chain Mariola Koszytkowska-Stawi¨½ska, Erik De Clercq, Jan Balzarini Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 2-amino-4-(4-fluorophenyl)-6-(pyridine-2-ylthio)-pyridine-3,5-dicarbonitrile C18H10N5FS ÏàËÆ¶È:56.2% Chemical & Pharmaceutical Bulletin 2013 61 1114-1120 An Efficient Green Multi-Component Reaction Strategy for the Synthesis of Highly Functionalised Pyridines and Evaluation of Their Antibacterial Activities Lakkireddy Srinivasula Reddy, Tirumalareddy Ram Reddy, Reddy Bodireddy Mohan, Avula Mahesh, Yeramanchi Lingappa, Nallagondu Chinna Gangi Reddy Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 2-amino-4-(4-bromophenyl)-6-(pyridine-2-ylthio)-pyridine-3,5-dicarbonitrile C18H10N5SBr ÏàËÆ¶È:56.2% Chemical & Pharmaceutical Bulletin 2013 61 1114-1120 An Efficient Green Multi-Component Reaction Strategy for the Synthesis of Highly Functionalised Pyridines and Evaluation of Their Antibacterial Activities Lakkireddy Srinivasula Reddy, Tirumalareddy Ram Reddy, Reddy Bodireddy Mohan, Avula Mahesh, Yeramanchi Lingappa, Nallagondu Chinna Gangi Reddy Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 2-(3,4-Difluorophenyl)-3,5,7-trihydroxy-4H-chromen-4-one C15H8F2O5 ÏàËÆ¶È:56.2% Journal of Agricultural and Food Chemistry 2012 60 6499-6506 Separation of Quercetin¡¯s Biological Activity from Its Oxidative Property through Bioisosteric Replacement of the Catecholic Hydroxyl Groups with Fluorine Atoms Suh Young Cho, Mi Kyoung Kim, Hyejung Mok, Hyunah Choo, and Youhoon Chong Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . eucomin ÏàËÆ¶È:56.2% China Journal of Chinese Materia Medica 2012 37 2105-2107 Chemical constituents and antibacterial activity contained in Caesalpinia millettii CHEN Ping; LEI Jun; XU Xudong; YANG Junshan Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 1,1'-diethyldicarboxylate-3,3'-bis(p-nitro-benzoyl)-7,7'-bis(indolizine) C36H26N4O10 ÏàËÆ¶È:56.2% Marine Drugs 2013 11 431-439 Novel One-Pot Green Synthesis of Indolizines Biocatalysed by Candida antarctica Lipases Rodica Mihaela Dinica, Bianca Furdui, Ioana Otilia Ghinea, Gabriela Bahrim, Simon Bonte and Martine Demeunynck Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . (E)-Methyl 4-(4-((Z)-3-methoxy-3-oxoprop-1-enyl)phenoxy)-2-methylbut-2-enoate C16H18O5 ÏàËÆ¶È:56.2% International Journal of Molecular Sciences 2013 14 22395-22408 New Benzo[c]phenanthridine and Benzenoid Derivatives,and Other Constituents from Zanthoxylum ailanthoides:Effects on Neutrophil Pro-Inflammatory Responses Ching-Yi Chung, Tsong-Long Hwang, Liang-Mou Kuo, Wen-Lung Kuo, Ming-Jen Cheng, Yi-Hsiu Wu, Ping-Jyun Sung, Mei-Ing Chung, and Jih-Jung Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 3-Cyano-6-(3-bromo-2-hydroxy-4-isopropoxyphenyl)-5-phenylpyridin-2(1H)-one C21H17BrN2O3 ÏàËÆ¶È:56.2% Chinese Journal of Chemistry 2013 31 1027-1032 Synthesis of 5,6-Diarylpyridin-2(1H)-ones from Isoflavones Mulin Zhu, Zunting Zhang, Dong Xue, Jinfeng Qiao, Yong Liang and Stanislaw F. Wnuk Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 6,8-¶þ¼×Ñõ»ù-2-¼×ËáÒÒõ¥»ù-4-¼×Ëá¼×õ¥»ù-àßø C16H17NO6 ÏàËÆ¶È:56.2% Chinese Journal of Organic Chemistry 2014 34 1437-1441 CuBr2-Catalyzed Three-Component Coupling for Synthesis of Quinoline-2,4-dicarboxyl Derivatives Wang, Kou Yu, Haofei Ding, Linfen Hu, Jianlin Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . N-(4-Chlorophenyl)-2-((2-((4-cyanophenyl)amino)-5-methylpyrimidin-4-yl)oxy)acetamide ÏàËÆ¶È:56.2% Bioorganic & Medicinal Chemistry 2015 23 624−631 Synthesis and biological evaluation of DAPY¨CDPEs hybrids as non-nucleoside inhibitors of HIV-1 reverse transcriptase Hai-Qiu Wu, Jin Yao, Qiu-Qin He, Wen-Xue Chen, Fen-Er Chen, Christophe Pannecouque, Erik De Clercq, Dirk Daelemans Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . methyl 4-benzyloxy-3-methoxyphenoxyacetate C17H18O5 ÏàËÆ¶È:56.2% Tetrahedron 2005 61 10061-10072 An efficient synthesis of benzofurans and their application in the preparation of natural products of the genus CaleaOriginal Research Article Mar¨ªa del Carmen Cruz, Joaqu¨ªn Tamariz Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . globulixanthone C C18H14O6 ÏàËÆ¶È:52.9% Phytochemistry 2002 61 181-187 Globulixanthones C, D and E:three prenylated xanthones with antimicrobial properties from the root bark of Symphonia globulifera Augustin E. Nkengfack, Pierre Mkounga, Michele Meyer,Zacharias T. Fomum, Bernard Bodo Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . Compound 25 ÏàËÆ¶È:52.9% Bioorganic & Medicinal Chemistry Letters 2004 14 2473-2476 Linker-modified quinoline derivatives targeting HIV-1 integrase: synthesis and biological activity Christophe B¨¦nard, Fatima Zouhiri, Marie Normand-Bayle, Mich¨¨le Danet, Didier Desmaële, Herv¨¦ Leh, Jean-François Mouscadet, Gladys Mbemba, Claire-Marie Thomas, Sabine Bonnenfant, Marc Le Bret, Jean d'Angelo Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-03-23 14:22:33














»Ø¸´´ËÂ¥
120