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13C NMR (151 MHz, CDCl3) ¦Ä14.19,29.41,29.74,31.03,31.67,31.72,31.97,56.24,61.11,70.63,103.73,103.95,106.50,114.78,117.06,125.85,127.44,138.70,143.81,145.37,146.69,147.54,154.98.

[ Last edited by tianxinyan on 2012-10-7 at 12:59 ]
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tianxinyan: ½ð±Ò+25, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл 2012-10-09 12:35:45
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1 .     smiranicin
C19H18O5     ÏàËÆ¶È:78.2%
Journal of Natural Products          2002          65          1754-1758
Leishmanicidal and Antiplasmodial Activity of Constituents of Smirnowia iranica
Majid Sairafianpour,Oliver Kayser, Jette Christensen, Mohammad Asfa, Matthias Witt, Dan Stærk, and Jerzy W. Jaroszewski
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     3-[3,4-Dihydro-8-(2-propenyl)-2H-furo[2,3-h]-1-benzopyran-3-yl]-2,6-dimethoxyphenol
    ÏàËÆ¶È:69.5%
Journal of Natural Products          2005          68          1500-1509
Rapid Extract Dereplication Using HPLC-SPE-NMR:Analysis of Isoflavonoids from Smirnowia iranica
Maja Lambert, Steen Honor Hansen, Majid Sairafianpour, and Jerzy W. Jaroszewski
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     compound 12b
C30H38O2S2     ÏàËÆ¶È:62.5%
European Journal of Organic Chemistry          2011                   569-577
Lewis-Acid-Mediated Domino Reactions of Bis(diacetoxymethyl)-Substituted Arenes and Heteroarenes
J. Arul Clement, Ramakrishnan Sivasakthikumaran, Arasambattu K. Mohanakrishnan, S. Sundaramoorthy and Devadasan Velmurugan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     compound 5c
C26H42O2     ÏàËÆ¶È:56.5%
Zeitschrift f¨¹r Naturforschung B          2004          59          233-240
Dialkoxy-Substituted, C1-Symmetric Metallocenes: Synthesis and Catalytic Behavior in the Propylene Polymerization Reaction
M. Schlögl and B. Rieger
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     8-prenylmucronulatol
C12H26O5     ÏàËÆ¶È:52.1%
Journal of Natural Products          2002          65          1754-1758
Leishmanicidal and Antiplasmodial Activity of Constituents of Smirnowia iranica
Majid Sairafianpour,Oliver Kayser, Jette Christensen, Mohammad Asfa, Matthias Witt, Dan Stærk, and Jerzy W. Jaroszewski
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     glyasperin H
    ÏàËÆ¶È:52.1%
Journal of Natural Products          2002          65          1754-1758
Leishmanicidal and Antiplasmodial Activity of Constituents of Smirnowia iranica
Majid Sairafianpour,Oliver Kayser, Jette Christensen, Mohammad Asfa, Matthias Witt, Dan Stærk, and Jerzy W. Jaroszewski
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     4''-hydroxyimperatorin 4''-O-¦Â-D-glucopyranoside
C22H24O10     ÏàËÆ¶È:52.1%
Chemical & Pharmaceutical Bulletin          1998          46          1404-1407
Coumarin Glycosides of Glehnia littoralis Root and Rhizoma
Junichi KITAJIMA,Chieko OKAMURA,Toru ISHIKAWA and Yasuko TANAKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     docosyl ferulate
C32H54O4     ÏàËÆ¶È:52.1%
Acta Pharmaceutica Sinica          1998          Vol 33          350-354
STUDIES ON CHEMICAL CONSTITUENTS OF TINOSPORA HAINANESIS
Guo Youying(Guo YY); Lin Lianbo(Lin LB) and Shen Jing(Shen J)
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     Ethyl 4-[(3a¦Á,4¦Á,9b¦Á)-8-methoxy-2,3,3a,4,5,9b-hexahydrofuro[3,2-c]quinolin-4-yl]-1-(4-nitrophenyl)-1H-pyrazole-3-carboxylate
C24H24N4O6     ÏàËÆ¶È:52.1%
Canadian Journal of Chemistry          2006          84          464-468
Chiral shift reagent catalyzed, diastereoselective imino Diels-Alder reaction - Synthesis of pyrazolyltetrahydroquinolines
Radhakrishnan Sridhar and Paramasivan T. Perumal
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     30,32,33,34-tetramethoxy-10,16,22,28-tetrakis(tert-butyl)-31-thiahexacyclo[24.3.1.1(3,6).1(8,12).1(14,18).1(20,24)]tetratriaconta-1(29),3(4),5,8(9),10,12(32),14(15),16,18(33),20(21),24(34),26(30),27-tetradecaene
C53H68O4S     ÏàËÆ¶È:52.1%
Journal of Heterocyclic Chemistry          2001          38          293-298
Synthesis and properties of calixarene analogs incorporating a thiophene unit in the macrocyclic ring
Kazuaki Ito, Yoshihiro Ohba, Takafumi Tamura, Tomoaki Ogata, Hajime Watanabe, Yasumitsu Suzuki, Takayuki Hara, Yukou Morisawa and Tyo Sone
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     Sphaerosin s1
    ÏàËÆ¶È:52.1%
Pharmazie          2002          57          75-76
Isoflavans from Sphaerophysa salsula
Zhong-Jun Ma - Bai-Ling Hou - Jin-Hui Wang - Xian Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     compound 4
    ÏàËÆ¶È:52.1%
Organic & Biomolecular Chemistry          2004          2          1827-1830
Viscosaline: new 3-alkyl pyridinium alkaloid from the Arctic sponge Haliclona viscosa
Christian A. Volk and Matthias Köck
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     5,7,5 '-trimethoxy-6-(30-hydroxy,30-methyl-trans-but-10-enyl)-3 ',4 '-methylenedioxy-flavone
C24H24O8     ÏàËÆ¶È:50%
Phytochemistry          1999          52          1705-1709
Prenylated flavones from Neoraputia paraensis
Jose Pio I. de Souz, Alberto C. Arrud, Gaspar D. Munoz, Mara S. P. Arrud, Adolfo H. Muller
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     Paniculacin
C26H35O6     ÏàËÆ¶È:50%
Journal of Asian Natural Products Research          2011          Vol.13,No.8          724-727
Paniculacin, a new coumarin derivative from Murraya paniculata
Sumayya Saeed, Shazia Shah, Rashad Mehmood and Abdul Malik
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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