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Âíβɼ: ½ð±Ò+8, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ·Ç³£¸Ðл ôôßÕ 2015-04-15 20:17:47
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1 .     Lycopoclavamine-A
C16H23NO2     ÏàËÆ¶È:100%
Tetrahedron          2011          67          6561-6567
Ten new fawcettimine-related alkaloids from three species of Lycopodium
Kazuaki Katakawa, Hiroko Mito, Noriyuki Kogure, Mariko Kitajima, Sumphan Wongseripipatana, Munehisa Arisawa, Hiromitsu Takayama
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     Dihydrolycopoclavamine-A
C16H25NO2     ÏàËÆ¶È:81.2%
Tetrahedron          2011          67          6561-6567
Ten new fawcettimine-related alkaloids from three species of Lycopodium
Kazuaki Katakawa, Hiroko Mito, Noriyuki Kogure, Mariko Kitajima, Sumphan Wongseripipatana, Munehisa Arisawa, Hiromitsu Takayama
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     buddledin C
    ÏàËÆ¶È:75%
Journal of Natural Products          2002          65          887-891
Suberosols A-D, Four New Sesquiterpenes with ¦Â-Caryophyllene Skeletons from a Taiwanese Gorgonian Coral Subergorgia suberosa
Guey-Horng Wang, Atallah F. Ahmed, Jyh-Horng Sheu, Chang-Yih Duh, Ya-Ching Shen, and Li-Tang Wang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     3-ketotrans-caryophyllene
    ÏàËÆ¶È:75%
Chemistry of Natural Compounds          2006          42          41-45
BUDDLEDIN C FROM Pulicaria prostrata AND SELECTIVE SYNTHESIS OF ITS EPOXY DERIVATIVE
D. T. Sadyrbekov, G. A. Atazhanova, A. T. Kulyyasov,V. A. Raldugin, Yu. V. Gatilov, M. M. Shakirov,T. T. Edil'baeva, K. M. Turdybekov, and S. M. Adekenov
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     Lycopoclavamine-B
C16H23NO3     ÏàËÆ¶È:75%
Tetrahedron          2011          67          6561-6567
Ten new fawcettimine-related alkaloids from three species of Lycopodium
Kazuaki Katakawa, Hiroko Mito, Noriyuki Kogure, Mariko Kitajima, Sumphan Wongseripipatana, Munehisa Arisawa, Hiromitsu Takayama
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     (1S,2S,5R,6S,8S)-8-methylene-1,4,4-trimethyltricyclo[6.2.1.0(2,5)]-undecane-6,12-diol
C15H26O2     ÏàËÆ¶È:75%
Journal of Natural Products          2013          76          1016-1024
Phytotoxic Activity and Metabolism of Botrytis cinerea and Structure¨CActivity Relationships of Isocaryolane Derivatives
Jociani Ascari, Maria Am¨¦lia Diamantino Boaventura, Jacqueline Aparecida Takahashi, Rosa Dur¨¢n-Patr¨®n, Rosario Hern¨¢ndez-Gal¨¢n, Antonio J. Mac¨ªas-S¨¢nchez, and Isidro G. Collado
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     7-methoxy-1,7-dimethyltricyclo[6.2.2.0(4,9)]dodecan-3-one
C15H24O2     ÏàËÆ¶È:75%
European Journal of Organic Chemistry          2006          2006          3181-3192
Towards the Total Synthesis of Vibsanin E, 15-O-Methylcyclovibsanin B,3-Hydroxyvibsanin E, Furanovibsanin A, and 3-O-Methylfuranovibsanin A
Brett D. Schwartz, David P. Tilly, Ralf Heim, Stefan Wiedemann, Craig M. Williams and Paul V. Bernhardt
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     A-homo-5¦Â-cholestane
C28H50     ÏàËÆ¶È:70.5%
Canadian Journal of Chemistry          1979          57          1550-1556
13C nuclear magnetic resonance studies. 85. 13C spectra of several ring-contracted and -expanded steroids
Vinod Dave, J. B. Stothers
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     11-Acetyloxy-1¦Á-hydroxy-1-epiprobotrydial
    ÏàËÆ¶È:70.5%
Journal of Chemical Ecology          1994          20          2631-2644
Synthesis and antifungal activity of analogues of naturally occurring botrydial precursors
Isidro G. Collado, Josefina Aleu, Antonio J. Mac¨ªas-S¨¢nchez, Rosario Hern¨¢ndez-Gal¨¢n
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     lycoposerramine-J
C16H25NO2     ÏàËÆ¶È:68.7%
Chemical & Pharmaceutical Bulletin          2003          51(10)          1163-1169
Ten New Lycopodium Alkaloids Having the Lycopodane Skeleton Isolated from Lycopodium serratum THUNB.
Hiromitsu TAKAYAMA,Kazuaki KATAKAWA,Mariko KITAJIMA, Kentaro YAMAGUCHI,and Norio AIMI
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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