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li7yan

Ìú³æ (СÓÐÃûÆø)

[ÇóÖú] ΢Æ×²éѯ

13C NMR: 11.98, 17,46, 18.19, 19.61, 24.08, 26.06, 27.29, 27.68, 28.30, 28.83, 29.86, 30.05, 32.96, 38.70, 38.96, 39.44, 40.82, 46.55, 47.18, 51.78, 56.58, 57.97, 61.34, 65.89, 66.72, 72.20, 212.24
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1 .     3¦Â-propionoxyimperialine
C30H47NO4     ÏàËÆ¶È:76.6%
Planta Medica          1998          64          172-174
Structure-Activity Relationships of Imperialine Derivatives and their Anticholinergic Activity
AttaurRahma, M. lqbal Choudhary, Afgan Farooq,Shazia Anjum, Jesse Baumgold, and Bilge Sener
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     12¦Á-Chloro-9¦Á,11¦Á-epoxy-5¦Á-stigmastan-3¦Â-ol
C29H49ClO2     ÏàËÆ¶È:71.4%
European Journal of Organic Chemistry          1993          1993          657-663
Pheromone Synthesis, CLI. Synthesis of Chlorinated Steroids Related to the Structures Proposed for Blattellastanosides A and B, the Aggregation Pheromone of the German Cockroach, Blattella germanica L.
Kenji Mori, Kunio Fukamatsu and Masaru Kido
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     3¦Â-butyroxyimperialine
C31H49NO4     ÏàËÆ¶È:70.9%
Planta Medica          1998          64          172-174
Structure-Activity Relationships of Imperialine Derivatives and their Anticholinergic Activity
AttaurRahma, M. lqbal Choudhary, Afgan Farooq,Shazia Anjum, Jesse Baumgold, and Bilge Sener
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     compound 4
     ÏàËÆ¶È:70%
Chemistry of Natural Compounds          1985          21          605-612
13C NMR SPECTRA OF A NUMBER OF PENTA- AND HEXACYCLIC TRITERPENOIDS DERIVED FROM GLYCYRRHETIC ACID
G. A. Tolstikov, L. M. Khalilov, L. A. Baltina, R. M. Kondratenko, A. A. Panasenko, and E. V. Vasil'eva
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     24¦Î-methylcholestane-3¦Â,5¦Á,6¦Â,25-tetrol
C28H50O4     ÏàËÆ¶È:67.8%
Acta Scientiarum Naturalium Universitatis Sunyatseni          1994          33(1)          123-126
Studies on the Marine Soft Coral Lobiphytum caledonense Tix Dur¢ò, Polyhydroxysteriods
Meng Yanhui, Su Jingyu, Zeng Longmei, Cui Yusheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     6¦Á-acetoxy-16¦Â,22-dihydroxy-3-ketoisohopane
C32H52O5     ÏàËÆ¶È:66.6%
Fitoterapia          2002          73          363-368
Triterpenes from Adiantum lunulactum
G. Brahmachari , D. Chatterjee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     (3¦Â,18¦Â,20¦Â)-3-amino-11-oxo-olean-12-en-29-oic acid hyd-rochloride
     ÏàËÆ¶È:66.6%
Bioorganic & Medicinal Chemistry          2010          18          7522-7541
Synthesis of novel 3-amino and 29-hydroxamic acid derivatives of glycyrrhetinic acid as selective 11¦Â-hydroxysteroid dehydrogenase 2 inhibitors
Christian Stanetty, Laszlo Czollner, Iris Koller, Priti Shah, Rawindra Gaware, Thierry Da Cunha, Alex Odermatt, Ulrich Jordis, Paul Kosma, Dirk Claßen-Houben
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     Epoxyinonotsudiol
C30H48O3     ÏàËÆ¶È:66.6%
Phytochemistry Letters          2012          5          480-485
Four new lanostane-type triterpenoids from Inonotus obliquus
Noriko Handa, Takeshi Yamada, Reiko Tanaka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     cyclopholidone
     ÏàËÆ¶È:65.5%
China Journal of Chinese Materia Medica          2004          29          47-49
Studies on chemical constituents of Pholidaota yunnanensid
BI Zhiming, WANG Zhengtao, XU Luoshan, XU Guojun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     imperialine ¦Â-N-oxide
C27H43O4N     ÏàËÆ¶È:64.2%
Planta Medica          1998          64          448-450
Isolation and Structure Elucidation of Alkaloids from the Bulb of Fritillaria wabuensis
Anjiang Zhang, Huayuan Wang, Xinyao Tang, Yong Zheng, Xiaohui Yi, and Kaibei Yu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     (1'S,5R/S) 7-Butyl-8,8-dimethyl-3-(1',2'-di-O-isopropylidene-1',2'-dihydroxyethyl)-6-oxo-1-oxa-2,7-diazaspiro-[4,4]non-2-ene
     ÏàËÆ¶È:64.2%
Molecules          1997          2          57-61
Synthesis of Spiroisoxazolines by 1, 3-Dipolar Cycloaddition
Peter Micuch, Lubor Fisera, Vladimir Ondrus and Peter Ertl
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     compound 2
     ÏàËÆ¶È:64.2%
Acta Pharmaceutica Sinica          1993          28          192-196
ISOLATION AND IDENTIFICATION OF YIBEINOSlDE B
YJ Xu DM Xu; DB Cui; EX Huang; XQ Jin; SY Liu and MM Yan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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