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ÍðÈçÇåÌÀ: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-06-06 09:22:37
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1 . 15,16-epoxy-3-palmitoyloxy-kauran-2-one C36H60O4 ÏàËÆ¶È:63.6% Phytochemistry 2004 65 1291-1298 Antibacterial diterpenes and their fatty acid conjugates from rice leaves Yoshiki Kono, Aya Kojima, Rieko Nagai, Manabu Watanabe,Takahiro Kawashima, Tsugu Onizawa, Tohru Teraoka, Minoru Watanab,Hiroyuki Koshino, Jun Uzawa, Yoshikatsu Suzuki, Akira Sakurai Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 5-normethylbudmunchiamine-K C30H62N4O ÏàËÆ¶È:62.5% Phytochemistry 1996 42 1211-1215 Spermine alkaloids from Albizia schimperana Geoffrey M. Rukunga, Peter G. Waterman Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 14-Normethylbudmunchiamine-A C30H62N4O ÏàËÆ¶È:62.5% Phytochemistry 1996 42 1211-1215 Spermine alkaloids from Albizia schimperana Geoffrey M. Rukunga, Peter G. Waterman Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 20R,24S-Epoxycycloartan-3¦Â,6¦Á,25-triol-16-one ÏàËÆ¶È:62.5% Chemistry of Natural Compounds 2010 46 407-411 Triterpene glycosides from Astragalus and their genins. LXXXVII. Chemical transformation of cycloartanes. IX. Partial synthesis of cycloasalgenin I. M. Isaev, D. A. Iskenderov and M. I. Isaev Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . ginsenoyne M C32H46O2 ÏàËÆ¶È:62.5% Heterocycles 2000 53 2451-2457 Three Diels-Alder Type Adducts, Ginsenoynes L, M, and N, from the Roots of Panax ginseng Kazuhiro Hirakura,* Kou Sugama, Makoto Morita, Kaoru Nakajima, Hiroshi Sasaki, Minoru Okada, and Hajime Sato Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . batzelladine H C35H56N6O3 ÏàËÆ¶È:60% The Journal of Organic Chemistry 1997 62 1814-1819 Batzelladines F−I, Novel Alkaloids from the Sponge Batzella sp.: Inducers of p56lck-CD4 Dissociation Ashok D. Patil, Alan J. Freyer, Paul B. Taylor, Brad Cart¨¦, Gary Zuber, Randall K. Johnson, and D. John Faulkner Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . budmunchiamine K C31H64N4O2 ÏàËÆ¶È:59.3% Journal of Natural Products 1996 59 850-853 New Macrocyclic Spermine (Budmunchiamine) Alkaloids from Albizia gummifera: With Some Observations on the Structure-Activity Relationships of the Budmunchiamines Geoffrey M. Rukunga and Peter G. Waterman Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 6'¦Î-hydroxybudmunchiamine K C28H58N4O ÏàËÆ¶È:59.3% Journal of Natural Products 1996 59 850-853 New Macrocyclic Spermine (Budmunchiamine) Alkaloids from Albizia gummifera: With Some Observations on the Structure-Activity Relationships of the Budmunchiamines Geoffrey M. Rukunga and Peter G. Waterman Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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