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wchen/199033

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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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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   Ì¼Æ×Ä£Äâͼ
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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   Ì¼Æ×Ä£Äâͼ
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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   Ì¼Æ×Ä£Äâͼ
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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   Ì¼Æ×Ä£Äâͼ
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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   Ì¼Æ×Ä£Äâͼ
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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   Ì¼Æ×Ä£Äâͼ
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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   Ì¼Æ×Ä£Äâͼ
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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   Ì¼Æ×Ä£Äâͼ
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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   Ì¼Æ×Ä£Äâͼ
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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   Ì¼Æ×Ä£Äâͼ
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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   Ì¼Æ×Ä£Äâͼ
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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   Ì¼Æ×Ä£Äâͼ
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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   Ì¼Æ×Ä£Äâͼ
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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   Ì¼Æ×Ä£Äâͼ
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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   Ì¼Æ×Ä£Äâͼ
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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   Ì¼Æ×Ä£Äâͼ
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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 Cyclization
Dr. Kenji Sugimoto, Kazuki Toyoshima, Shiori Nonaka, Kenta Kotaki, Dr. Hirofumi Ueda and Prof. Dr. Hidetoshi Tokuyama
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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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   Ì¼Æ×Ä£Äâͼ
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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   Ì¼Æ×Ä£Äâͼ
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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   Ì¼Æ×Ä£Äâͼ
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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   Ì¼Æ×Ä£Äâͼ
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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   Ì¼Æ×Ä£Äâͼ
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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   Ì¼Æ×Ä£Äâͼ
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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   Ì¼Æ×Ä£Äâͼ
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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   Ì¼Æ×Ä£Äâͼ
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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   Ì¼Æ×Ä£Äâͼ
2Â¥2014-11-04 19:47:00
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