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1 . hygrocin D C28H31NO8 ÏàËÆ¶È:67.8% Journal of Natural Products 2013 76 2175-2179 Hygrocins C¨CG, Cytotoxic Naphthoquinone Ansamycins from gdmAI-Disrupted Streptomyces sp. LZ35 Chunhua Lu, Yaoyao Li, Jingjing Deng, Shanren Li, Yan Shen, Haoxin Wang, and Yuemao Shen Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . hygrocin E C28H31NO8 ÏàËÆ¶È:60.7% Journal of Natural Products 2013 76 2175-2179 Hygrocins C¨CG, Cytotoxic Naphthoquinone Ansamycins from gdmAI-Disrupted Streptomyces sp. LZ35 Chunhua Lu, Yaoyao Li, Jingjing Deng, Shanren Li, Yan Shen, Haoxin Wang, and Yuemao Shen Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . Hygrocin F C28H31NO8 ÏàËÆ¶È:60.7% Journal of Natural Products 2013 76 2175-2179 Hygrocins C¨CG, Cytotoxic Naphthoquinone Ansamycins from gdmAI-Disrupted Streptomyces sp. LZ35 Chunhua Lu, Yaoyao Li, Jingjing Deng, Shanren Li, Yan Shen, Haoxin Wang, and Yuemao Shen Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (S,Z)-tert-Butyl(1-(4-methoxybenzyloxy)undec-3-en-2-yloxy) diphenylsilane C35H48O3Si ÏàËÆ¶È:55.5% Tetrahedron 2012 68 262-271 A flexible organocatalytic enantioselective synthesis of heptadeca-1-ene-4,6-diyne-3S,8R,9S,10S-tetrol and its congeners Gullapalli Kumaraswamy, Kadivendi Sadaiah Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 2-{5-(4-methoxyphenethoxy)-1-{5-[4-(methylthio)-phenyl]pentyl}-1H-indole-3-yl}ethanamine hydrochloride C31H39N2O2SCl ÏàËÆ¶È:55.5% Bioorganic & Medicinal Chemistry 2010 18 3387-3402 Serotonin derivatives as a new class of non-ATP-competitive receptor tyrosine kinase inhibitors Anita B¨¹ttner, Thomas Cottin, Jing Xu, Lito Tzagkaroulaki, Athanassios Giannis Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . cytochalasin J ÏàËÆ¶È:55.5% Tetrahedron 1989 45 2323-2335 Six new 10-pheynl-[11]cytochalasans, cytochalasins N - S from phomopsis SP. Yoshihiko Izawa, Takashi Hirose, Takako Shimizu (n¨¦e Tomioka), Kiyotaka Koyama, Shinsaku Natori Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 5-(4-Methoxyphenyl)-6-methyl-8-(5'-methoxy-3'-phenyl-1H-indol-2'-carbonyl)-1,3-dihydro-2,4-dithioxo-pyrazolo[2,3-c]-1,4-dihydropyrano[2,3-e]pyrimidine C32H25N5O4S2 ÏàËÆ¶È:55.5% Journal of Heterocyclic Chemistry 2014 51 303-314 Synthesis and Biological Activities of Some New Annulated Pyrazolopyranopyrimidines and Their Derivatives Containing Indole Nucleus Anand R. Saundane, Prabhaker Walmik, Manjunatha Yarlakatti, Vijaykumar Katkar and Vaijinath A. Verma Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . compound 11c C29H38O4 ÏàËÆ¶È:53.5% Steroids 2001 66 623-635 Neighboring group participation. Part 14. The preparation of the four stereoisomers of 16-hydroxymethyl-5¦Á-androstane-3¦Â,17-diol P¨¢l Tapolcs¨¢nyi, J¨¢nos Wölfling, Gyula Schneider Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . (1S,4R,5S,6R,7R,8R,9S,10S)-1,8,9-tribenzoyloxy-6-hydroxydihydro-¦Â-agarofuran C36H38O8 ÏàËÆ¶È:53.3% Journal of Natural Products 2008 71(6) 1005-1010 Cytotoxic Dihydroagarofuranoid Sesquiterpenes from the Seeds of Celastrus orbiculatus Yingdong Zhu, Zehong Miao, Jian Ding, and Weimin Zhao Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . (Z)-2-[6'-(6-(4-((5-dimethylaminonaphthalene-1-sulfonyl)amino))hexanamide)-¦Â-D-galactopyranosyloxy]-3-p-hydroxyphenylacrylate C33H40N3O11S ÏàËÆ¶È:53.3% Tetrahedron Letters 2001 42 3869-3872 Direct observation of the target cell for leaf-movement factor using novel fluorescence-labeled probe compounds: fluorescence studies of nyctinasty in legumes. Part 1 Minoru Ueda, Yoko Wada, Shosuke Yamamura Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . micromonosporin A C26H37O4N ÏàËÆ¶È:51.8% Chemistry & Biodiversity 2004 Vol.1 640 Micromonosporin A, a Novel 24-Membered Polyene Lactam Macrolide from Micromonospora sp. Isolated from Peat Swamp Forest Chitti Thawai, Prasat Kittakoop, Somboon Tanasupawat, Khanit Suwanborirux, Kanlayanee Sriklung, and Yodhathai Thebtaranonth Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . isovouacapenol A ÏàËÆ¶È:51.8% Chemical & Pharmaceutical Bulletin 2003 51(10) 1208-1210 A New Furanoid Diterpene from Caesalpinia pulcherrima Consolacion Y. RAGASA,Jerome GANZON,Joy HOFILEÑA,Benjie TAMBOONG,and John A. RIDEOUT Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . isovouacapenol A C27H32O4 ÏàËÆ¶È:51.8% Journal of Natural Products 2002 65 1107-1110 New Furanoid Diterpenes from Caesalpinia pulcherrima Consolacion Y. Ragasa,Joy G. Hofileña,and John A. Rideout Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . (2''S,3''R)-dibromo-7-epi-cephalomannine ÏàËÆ¶È:51.8% Journal of Natural Products 1998 61 57-63 Synthesis and Separation of Potential Anticancer Active Dihalocephalomannine Diastereomers from Extracts of Taxus yunnanensis Ramesh C. Pandey, Luben K. Yankov, Alexander Poulev, Raghu Nair, and Salvatore Caccamese Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . cytochalasin Z10 C28H37NO5 ÏàËÆ¶È:51.8% Chemistry & Biodiversity 2009 6 739-745 Cytotoxic Cytochalasin Metabolites of Endophytic Endothia gyrosa Shu Xu, Hui Ming Ge, Yong Chun Song, Yao Shen, Hui Ding, and Ren Xiang Tan Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 3-O-benzoate C36H42O10 ÏàËÆ¶È:51.8% Chemical & Pharmaceutical Bulletin 1997 45 152-160 Studies on the Constituents of Scutellaria Species. XVIII. Structures of Neoclerodane-Type Diterpenoids from the Whole Herb of Scutellaria rivularis WALL. Haruhisa KIZU,Yoshitaka IMOTO,Tsuyoshi TOMIMORI,Tohru KIKUCHI,Shigetoshi KADOTA and Koji TSUBONO Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . hypochoeroside F ÏàËÆ¶È:51.8% Phytochemistry 1989 28 1919-1924 Sesquiterpene glucosides and a phenylbutanoid glycoside from Hypochoeris radicata Kuniko Ohmura,Toshio Miyase,Akira Ueno Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . compound 8a ÏàËÆ¶È:51.8% Heterocycles 2010 80 1197-1213 Synthesis and Properties of Dicarboximide Derivatives of Perylene and Azaperylene Yukinori Nagao, Tatsurou Yoshida, Koji Arimitsu, and Kozo Kozawa Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 2-{5-(4-hydroxyphenethoxy)-1-{5-[4-(methylthio)-phenyl]pentyl}-1H-indole-3-yl}ethanamine hydrochloride C29H35N2O2SCl ÏàËÆ¶È:51.8% Bioorganic & Medicinal Chemistry 2010 18 3387-3402 Serotonin derivatives as a new class of non-ATP-competitive receptor tyrosine kinase inhibitors Anita B¨¹ttner, Thomas Cottin, Jing Xu, Lito Tzagkaroulaki, Athanassios Giannis Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . epoxycytochalasin J ÏàËÆ¶È:51.8% Tetrahedron 1989 45 2323-2335 Six new 10-pheynl-[11]cytochalasans, cytochalasins N - S from phomopsis SP. Yoshihiko Izawa, Takashi Hirose, Takako Shimizu (n¨¦e Tomioka), Kiyotaka Koyama, Shinsaku Natori Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . N-(1-hexylheptyl)-9,10-bis(propyloxycarbonyl)perylene-3,4-dicarboximide C43H49NO6 ÏàËÆ¶È:51.8% European Journal of Organic Chemistry 2011 707-712 Room-Temperature Columnar Liquid-Crystalline Perylene Imido-Diesters by a Homogeneous One-Pot Imidification¨CEsterification of Perylene-3,4,9,10-tetracarboxylic Dianhydride Julien Kelber, Harald Bock, Olivier Thiebaut, Eric Grelet and Heinz Langhals Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . (2S,2'R,3R,3'E,4E,8E,10E)-1-O-¦Â-D-glucopyranosyl-2-N-(2'-hydroxy-3'-octadecenoyl)-3-hydroxy-9-methyl-4,8,10-sphingatrienine C43H77NO9 ÏàËÆ¶È:51.8% Lipids 2004 39 667-673 Antibacterial and xanthine oxidase inhibitory cerebrosides from Fusarium sp. IFB-121, and endophytic fungus in Quercus variabilis R. G. Shu, F. W. Wang, Y. M. Yang, Y. X. Liu and R. X. Tan Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . compound ÏàËÆ¶È:51.8% Journal of the American Chemical Society 2004 126 3704-3705 Total Synthesis and Structural Revision of (+)-Amphidinolide W Arun K. Ghosh and Gangli Gong Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . compound 22 ÏàËÆ¶È:51.8% Journal of the American Chemical Society 2004 126 3704-3705 Total Synthesis and Structural Revision of (+)-Amphidinolide W Arun K. Ghosh and Gangli Gong Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . 2-(4-tert-butylphenyl)-1-heptylpyrido[2,3-b]quinoxalin-4(1H)-one C28H33N3O ÏàËÆ¶È:51.8% Tetrahedron 2013 69 2309-2318 Efficient synthesis of novel benzo[1,8]naphthyridin-4(1H)-ones and pyrido[2,3-b]quinoxalin-4(1H)-ones from alkynones and primary amines Viktor O. Iaroshenko, Muhammad Zahid, Satenik Mkrtchyan, Ashot Gevorgyan, Kai Altenburger, Ingo Knepper, Alexander Villinger, Vyacheslav Ya. Sosnovskikh, Peter Langer Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . dianthin A C33H43N7O8 ÏàËÆ¶È:51.8% Chemical Papers 2008 62 527-535 Synthesis and biological activity of a cyclic hexapeptide from Dianthus superbus Rajiv Dahiya Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . PGE2 bisphosphonate ester conjugate C57H66P2O12 ÏàËÆ¶È:51.8% Bioorganic & Medicinal Chemistry 1999 7 901-919 Prostaglandin E2-bisphosphonate conjugates: potential agents for treatment of osteoporosis Laurent Gil, Yongxin Han, Evan E. Opas, Gideon A. Rodan, R¨¦jean Ruel, J.Gregory Seedor, Peter C. Tyler, Robert N. Young Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . (11aS)-10-Octyl-7-(p-tolyl)-2,3-dihydro-1H-pyrrolo[2,1-c][1,4]benzodiazepine-5,11(10H,11aH)-dione C27H36N2O2 ÏàËÆ¶È:51.8% Journal of Heterocyclic Chemistry 2014 51 423-431 Syntheses of N10-substituted 7-Arylpyrrolo[2,1-c]-[1,4]benzodiazepine-5,11-diones Anika Sabine Lindner, Egor Geist, Mimoza Gjikaj and Andreas Schmidt Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . (15S)-11-deoxypentahomo-3-trans,23-trans-diene-prostaglandin E3 ÏàËÆ¶È:51.8% Chemistry of Natural Compounds 1985 21 293-297 13C NMR spectra of biologically active compounds. I. ¦Á-Homologs of 11-deoxyprostaglandin E1 G. A. Tolstikov, L. M. Khalilov, A. A. Panasenko, F. A. Valeev, M. S. Niftakhov Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . compound 14 ÏàËÆ¶È:51.7% Phytochemistry 2001 58 463-474 Semisynthetic derivatives of ent-kauranes and their antifeedant activity Maurizio Bruno, Sergio Rosselli, Ivana Pibiri, Franco Piozzi,Maria Luisa Bond¨¬, Monique S.J. Simmonds Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . Angulatueoid H(1¦Â,6¦Á-Diacetoxy-8¦Â,9¦Â-dibenzoyloxy-dihydro-¦Â-agarofuran) C33H38O11 ÏàËÆ¶È:51.7% Phytochemistry 1992 31 4219-4222 Iridoid glycosides from Penstemon species: A C-5, C-9 trans iridoid and C-8 epimeric pairs Tommaso A. Foderaro, Frank R. Stermitz Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . compound 2 ÏàËÆ¶È:51.7% The Journal of Antibiotics 1993 46 1390-1396 DELAMINOMYCINS, NOVEL EXTRACELLULAR MATRIX RECEPTOR ANTAGONISTS V. BIOSYNTHESIS MITSUHIRO UENO, IHOMI YOSHINAGA, MASAHIDE AMEMIYA, TETSUYA SOMENO, HIRONOBU IINUMA, MASAAKI ISHIZUAKA, TOMIO TAKEUCHI Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . euphoheliosnoid C C33H42O10 ÏàËÆ¶È:51.6% Planta Medica 2005 71 283-286 Three New Jatrophone-Type Diterpenoids from Euphorbia helioscopia Zhang, Wen; Guo, Yue-Wei Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . divergolide D C31H35NO8 ÏàËÆ¶È:51.6% Angewandte Chemie International Edition 2011 50 1630-1634 Divergolides A¨CD from a Mangrove Endophyte Reveal an Unparalleled Plasticity in ansa-Macrolide Biosynthesis Ling Ding, Armin Maier, Heinz-Herbert Fiebig, Helmar G rls, Wen-Han Lin, Gundela Peschel, and Christian Hertweck Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . (3aS,4S,5R,6R,7R,7aS)-2,2-Dimethyl-7-(4-methylphenyl(2-propynyl)sulfonamido)-4-(tertbutyldimethylsilyloxy)-5-phenylcarbonyloxy-6-(1-ethynyl)perhydro-1,3-benzodioxole C34H43NO7SSi ÏàËÆ¶È:50% Canadian Journal of Chemistry 2006 84 1313-1337 Cyclotrimerization approach to unnatural structural modifications of pancratistatin and other amaryllidaceae constituents - Synthesis and biological evaluation1 Tomas Hudlicky, Michael Moser, Scott C. Banfield, Uwe Rinner, Jean-Charles Chapuis, and George R. Pettit Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . compound 5a C30H37NO9 ÏàËÆ¶È:50% Tetrahedron 2008 64 7594-7604 A novel approach to the taxane ABC ring system through chemical conversion from C19-diterpenoid alkaloid deltaline Chun-Lan Zou, Le Cai, Hong Ji, Guang-Bo Xie, Feng-Peng Wang, Xi-Xian Jian, Lei Song, Xiao-Yu Liu, Dong-Lin Chen, Qiao-Hong Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . (¡À)-methyl 7-[3¦Á-hydroxy-2¦Â-[6-(2-hydroxy-(E)-cyclopentylidene)-4-methyl-1(E),4(E)-hexadienyl]-5-oxo-1¦Á-cyclopentyl]-4(Z)-heptenoate C25H36O5 ÏàËÆ¶È:50% Journal of Medicinal Chemistry 1990 33 2784-2793 Chemistry and structure-activity relationships of C-17 unsaturated 18-cycloalkyl and cycloalkenyl analogs of enisoprost. Identification of a promising new antiulcer prostaglandin P. W. Collins, A. F. Gasiecki, W. E. Perkins, G. W. Gullikson, R. G. Bianchi, S. W. Kramer, J. S. Ng, E. E. Yonan, L. Swenton, Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . (E)-2-(4-cinnamylpiperazin-1-yl)-N-(1-(4-fluorophenyl)-4,5-dihydro-[1,2,4]triazolo[4,3-a]quinolin-7-yl)acetamide C31H31FN6O ÏàËÆ¶È:50% Archiv der Pharmazie 2012 345 980-988 Synthesis and Positive Inotropic Evaluation of (E)-2-(4-Cinnamylpiperazin-1-yl)-N-(1-substituted-4,5-dihydro-[1,2,4]triazolo[4,3-a]quinolin-7-yl)acetamides Yan Wu, Long-Xu Ma, Tian-Wei Niu, Fan-Ling Meng, Xun Cui and Hu-Ri Piao Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . compound 13 C32H54O9SiS ÏàËÆ¶È:50% Chemistry-A European Journal 1996 2 847-868 Total Synthesis of Swinholide A, Preswinholide A, and Hemiswinholide A K. C. Nicolaou, A. P. Patron, K. Ajito, P. K. Richter, H. Khatuya, P. Bertinato, R. A. Miller and M. J. Tomaszewski Structure 13C NMR ̼Æ×Ä£Äâͼ |

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