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wchen/199033½ð³æ (СÓÐÃûÆø)
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| 13C NMR (126 MHz, cdcl3) ¦Ä 190.64, 177.23, 131.03, 130.15, 127.16, 126.72, 66.98, 60.56, 42.37, 38.76, 35.83, 33.65, 29.82, 28.43, 27.47, 22.61, 18.07. |
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wchen/199033: ½ð±Ò+10, ¡ïÓаïÖú 2014-11-04 20:22:31
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²éѯ½á¹û£º¹²²éµ½193¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . Equisetin C22H31NO4 ÏàËÆ¶È:72.7% Tetrahedron Letters 1998 39 2243-2246 Equisetin and a novel opposite stereochemical homolog phomasetin, two fungal metabolites as inhibitors of HIV-1 integrase Sheo B. Singh, Deborah L. Zink, Michael A. Goetz, Anne W. Dombrowski, Jon D. Polishook, Daria J. Hazuda Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . (2R,3R)-3-Benzyl-2,4-dihydroxy-3-methyl-N-(3-oxo-3-(pentylamino)propyl)butanamide C20H32N2O4 ÏàËÆ¶È:60% Bioorganic & Medicinal Chemistry 2011 19 2696-2706 Geminal dialkyl derivatives of N-substituted pantothenamides: Synthesis and antibacterial activity T. Olukayode Akinnusi, Kenward Vong, Karine Auclair Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . (4R,5R,8S)-4,5-epoxycaryophyllan-13-ol C14H23O2 ÏàËÆ¶È:58.8% Journal of Natural Products 1999 62 41-44 Biotransformation of Caryophyllene Oxide by Botrytis cinerea Rosa Duran, Elena Corrales, Rosario Hern¨¢ndez-Gal¨¢n, and Isidro G. Collado Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 12-isobutyryloxy-demethoxyencecalin ÏàËÆ¶È:58.8% Phytochemistry 1992 31 1070-1072 Chromenes from Arnica sachalinensis and A. amplexicaulis Claus M. Pa¦Âreiter, G¨¹nter Willuhn, Alois Steigel, Uwe Matthiesen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 3-Phenyl-5-[(8Z,11R)-11-hydroxyheptadec-8-enyl]-1H-1,2,4-triazole ÏàËÆ¶È:58.8% Archiv der Pharmazie 2008 341 714-720 Synthesis,Antibacterial and Antifungal Activity of Some Novel 3,5-Disubstituted-1H-1,2,4-triazoles Shweta Sharma, Saloni Gangal, Abdul Rauf and Maryam Zahin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 3-Pheny-5-[(8R,11Z)-8-Hydroxyheptadec-11-enyl]-1H-1,2,4-triazole ÏàËÆ¶È:58.8% Archiv der Pharmazie 2008 341 714-720 Synthesis,Antibacterial and Antifungal Activity of Some Novel 3,5-Disubstituted-1H-1,2,4-triazoles Shweta Sharma, Saloni Gangal, Abdul Rauf and Maryam Zahin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . 2-(Methylhydrazono)-3-(2-oxo-1-azepanyl)propiophenon C16H21N3O2 ÏàËÆ¶È:58.8% Zeitschrift f¨¹r Naturforschung B 2003 58 885-902 a-Dicarbonylmonohydrazones and their Acylderivatives as Nucleophiles and Neighbouring Groups (In German) H. Möhrle and G. Keller Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . 1,2,3,4,4a,9a-hexahydro-2,4-methano-3,3-dimethyl-9H-thioxanthene-4a-carbaldehyde C17H20OS ÏàËÆ¶È:58.8% Journal of Heterocyclic Chemistry 2012 49 516-520 Stereoselective Synthesis of Polycyclic Thiopyrans Herbert Meier, Michael Schmidt, Axel Mayer, Dieter Schollmeyer and Bernhard Beile Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . (6R)-hydroxy-¦Á-humulene ÏàËÆ¶È:58.8% Russian Journal of Bioorganic Chemistry 2010 36 899-908 Extractive Compounds of Birch Buds (Betula pendula Roth.): II.Carbonyl Compounds and Oxides.Esters D. N. Vedernikov and V. I. Roshchin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . salvidorol C19H26O4 ÏàËÆ¶È:57.8% Phytochemistry 2006 67 424-428 Salvidorol, a nor-abietane diterpene with a rare carbon skeleton and two abietane diterpene derivatives from Salvia dorrii Ahmed A. Ahmed, Abou El-Hamd H. Mohamed, Joe Karchesy, Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . N-[11-amino-1-benzyl-1-(N,N-dimethylcarbamoyl)undecyl]benzamide ÏàËÆ¶È:57.8% Heterocycles 2009 79 985-1005 Synthesis of Macrocyclic Lactams from 2-(¦Ø-Aminoalkyl)-2-benzoylamino-3-phenyl-N,N-dimethylpropanamides via Direct Amide Cyclization Stephan P. Fritschi, Anthony Linden, and Heinz Heimgartner Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . 8(SR)-iodo-1-phenyl-2(SR)-p-tolyl-(2aRS,5aRS,8aRS,9aSR)-octa-hydropyrrolo[4,3,2-de]isoquinoline-3,5-dione C23H23IN2O2 ÏàËÆ¶È:57.8% European Journal of Organic Chemistry 2011 2697-2704 ¦Â-Lactam-Synthon-Interceded, Facile, One-Pot, Diastereoselective Synthesis of Functionalized Tetra/Octahydroisoquinolone Derivatives Raghu Raj, Vishu Mehra, Pardeep Singh, Vipan Kumar, Gaurav Bhargava, Mohinder P. Mahajan, Sachin Handa and LeGrande M. Slaughter Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . epi-trichosetin C21H29NO4 ÏàËÆ¶È:57.1% The Journal of Antibiotics 2013 66 549-554 Epi-trichosetin, a new undecaprenyl pyrophosphate synthase inhibitor, produced by Fusarium oxysporum FKI-4553 Junji Inokoshi, Naoki Shigeta, Takashi Fukuda, Ryuji Uchida, Kenichi Nonaka, Rokurou Masuma and Hiroshi Tomoda Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . trichosetin C21H29NO4 ÏàËÆ¶È:57.1% The Journal of Antibiotics 2013 66 549-554 Epi-trichosetin, a new undecaprenyl pyrophosphate synthase inhibitor, produced by Fusarium oxysporum FKI-4553 Junji Inokoshi, Naoki Shigeta, Takashi Fukuda, Ryuji Uchida, Kenichi Nonaka, Rokurou Masuma and Hiroshi Tomoda Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . (5R)-5-(4-{(1S,5R)-1-hydroxy-5-[(2R,3E)-2-hydroxypent-3-en-1-yl]-4-oxocyclopent-2-en-1-yl}butyl)dihydrofuran-2(3H)-one C18H26O5 ÏàËÆ¶È:55.5% Journal of Natural Products 2008 71(4) 701-705 Chromomoric Acid Derivatives from Tectona philippinensis Consolacion Y. Ragasa, Myrna M. Tepora, Dinah H. Espinelli, Emelina H. Mandia, and John A. Rideout Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . 2(SR)-(4-chlorophenyl)-8(SR)-iodo-1-phenyl-(2aRS,5aRS,8aRS,9a-SR)-octahydropyrrolo[4,3,2-de]isoquinoline-3,5-dione 22H20ClIN2O2 ÏàËÆ¶È:55.5% European Journal of Organic Chemistry 2011 2697-2704 ¦Â-Lactam-Synthon-Interceded, Facile, One-Pot, Diastereoselective Synthesis of Functionalized Tetra/Octahydroisoquinolone Derivatives Raghu Raj, Vishu Mehra, Pardeep Singh, Vipan Kumar, Gaurav Bhargava, Mohinder P. Mahajan, Sachin Handa and LeGrande M. Slaughter Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . (-)-rhazinilam C19H22N2O ÏàËÆ¶È:55.5% Angewandte Chemie International Edition 2013 52 7168-7171 Protecting-Group-Free Total Synthesis of (− -Rhazinilam and (− -Rhazinicine using a Gold-Catalyzed Cascade CyclizationDr. Kenji Sugimoto, Kazuki Toyoshima, Shiori Nonaka, Kenta Kotaki, Dr. Hirofumi Ueda and Prof. Dr. Hidetoshi Tokuyama Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . compound 2d ÏàËÆ¶È:55.5% Magnetic Resonance in Chemistry 2012 50 823-828 1H, 13C and 15N NMR assignments for N- and O-acylethanolamines, important family of naturally occurring bioactive lipid mediators Roberta Ottria, Silvana Casati and Pierangela Ciuffreda Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . 2-¼×»ù-7,9-ʮһ¶þÏ¡Ëá¸ýõ¥ C19H34O2 ÏàËÆ¶È:55.5% Journal of Anhui Agricultural Sciences 2009 37 11001-11002 Study on the Chemical Components in the Roots of Anthriscus sylvestris WANG Yue-feng et al Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . kopsiyunnanine C3 C20H24N2O2 ÏàËÆ¶È:55% Journal of Natural Products 2009 72 204-209 Rhazinilam and Quebrachamine Derivatives from Yunnan Kopsia arborea Yuqiu Wu,Mayu Suehiro, Mariko Kitajima, Takeshi Matsuzaki, Shusuke Hashimoto,Masato Nagaoka,Rongping Zhang,and Hiromitsu Takayama Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . 3¦Â,19-dihydroxylabda-8(17),11E-dien-16,15-olide C20H30O4 ÏàËÆ¶È:55% Journal of Natural Products 2006 69 689-691 Neuroprotective Diterpenes from the Fruiting Body of Antrodia camphorata Cheng-Chi Chen, Young-Ji Shiao, Ruei-Da Lin, Yi-Yuan Shao,Min-Nan Lai, Chun-Ching Lin, Lean-Teik Ng, and Yueh-Hsiung Kuo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . 13-epi-3¦Â,19-dihydroxylabda-8(17),11E-dien-16,15-olide C20H30O4 ÏàËÆ¶È:55% Journal of Natural Products 2006 69 689-691 Neuroprotective Diterpenes from the Fruiting Body of Antrodia camphorata Cheng-Chi Chen, Young-Ji Shiao, Ruei-Da Lin, Yi-Yuan Shao,Min-Nan Lai, Chun-Ching Lin, Lean-Teik Ng, and Yueh-Hsiung Kuo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . 1¦Â,10¦Â-epoxy-2-oxofagonene C20H3O4 ÏàËÆ¶È:55% Planta Medica 1997 63 374-376 Erythroxan Diterpenes from Fagonia glutinosa Maged S. Abdel-Kader, Abdallah A. Omar, and Frank R. Stermitz Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . compound 14 C22H27NO3 ÏàËÆ¶È:55% Tetrahedron Letters 2003 44 2549-2552 Toward the synthesis of tetrodecamycin: asymmetric synthesis of a direct precursor of the C6---C18 trans-decalin portion Franz F Paintner, Gerd Bauschke, Kurt Polborn Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . N-butyloxycarbonyl-3-[4-(3,4,4-trimethyl-2,5-dioxo-imidazolidin-1-yl-methyl)-phenyl]-5-iso-butyl-thiophene-2-sulfonamide C26H35N3O6S2 ÏàËÆ¶È:55% Bioorganic & Medicinal Chemistry 2010 18 4570-4590 Selective angiotensin II AT2 receptor agonists with reduced CYP 450 inhibition A.K. Mahalingam, Yiqian Wan, A.M.S. Murugaiah, Charlotta Wallinder, Xiongyu Wu, Bianca Plouffe, Milad Botros, Fred Nyberg, Anders Hallberg, Nicole Gallo-Payet, Mathias Alterman Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . CJ-17,572 C21H31NO4 ÏàËÆ¶È:55% The Journal of Antibiotics 2002 55 19-24 A Novel Antibiotic CJ-17, 572 from a Fungus, Pezicula sp. YUTAKA SUGIE,KOEN A. DEKKER,TAISUKE INAGAKI,YOON-JEONG KIM,TATSUO SAKAKIBARA,SHINICHI SAKEMI,AKEMI SUGIURA,LORI BRENNAN,JOAN DUIGNAN,JOYCE A. SUTCLIFFE and YASUHIRO KOJIMA Structure 13C NMR ̼Æ×Ä£Äâͼ |
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