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»¯ºÏÎï34£º13C NMR (151 MHz, MeOD) ¦Ä 212.95, 207.96, 153.11, 152.63, 139.33, 137.26, 135.09, 134.42, 128.48, 128.32, 127.35, 127.02, 118.64, 117.31, 53.51, 49.72, 48.59, 47.80, 40.55, 32.15, 31.53, 28.97, 28.75, 28.19, 27.96, 27.94, 24.09, 23.25, 23.20, 23.16, 21.02, 20.94, 20.65, 20.22

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¹ÈÔÆ·É: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú, ·Ç³£¸Ðл 2015-04-05 11:14:32
1 .     (1R,3aR,4R,5S,7aR)-5-(N-benzyl-N-pent-4-enylami-no)-1-((R)-1,5-dimethylhexyl)-3a,7a-dimethyloctahydroinden-4-ol
    ÏàËÆ¶È:55.8%
Bioorganic & Medicinal Chemistry          2013          21          1925-1943
Stereoselective synthesis of a new class of potent and selective inhibitors of human ¦¤8,7-sterol isomerase
Mathias König, Christoph M¨¹ller, Franz Bracher
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     3,12-Diacetyl-8-nicotinyl-7-phenylacetyl 19-acetoxyingol
C40H46O12N     ÏàËÆ¶È:54.2%
Bioorganic & Medicinal Chemistry          1996          4          1679-1683
New 19-acetoxyingol diterpenes from the latex of Euphorbia poisonii (Euphorbiaceae)
Majekodunmi O. Fatope, Lu Zeng, Joseph E. Ohayagha, Jerry L. McLaughlin
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     (S)-Methyl 2-((2S,3S,Z)-1-((S)-2-benzamido-6-((Z)-2,3-bis(tert-butoxycarbonyl)guanidino)hexanoyl)-4-ethylidene-3-methylpyrrolidine-2-carboxamido)-4-methyl pentanoate
C39H60N6O9     ÏàËÆ¶È:54.2%
Tetrahedron          2012          68          1918-1925
Rhodium-catalyzed reductive cyclization of 1,6-enynes and stereoselective synthesis of the putative structure of lucentamycin A and its stereoisomers
Young Jin Ham, Hana Yu, Nam Doo Kim, Jung-Mi Hah, Khalid B. Selim, Hwan Geun Choi, Taebo Sim
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     Diaporthalasin
C32H39NO3     ÏàËÆ¶È:52.9%
Phytochemistry Letters          2014          10          5-9
An antibacterial cytochalasin derivative from the marine-derived fungus Diaporthaceae sp. PSU-SP2/4
Nanthaphong Khamthong, Vatcharin Rukachaisirikul, Souwalak Phongpaichit, Sita Preedanon, Jariya Sakayaroj
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     3-Hydroxy-1,3,5(10)-estratrien-17¦Â-O,17¦Á-(3' (R/S)-allylbutanolactone
C25H32O3     ÏàËÆ¶È:52.6%
Steroids          2004          69          325-342
Inhibition of type 2 17¦Â-hydroxysteroid dehydrogenase by estradiol derivatives bearing a lactone on the D-ring: structure¨Cactivity relationships
Patrick Bydal, Serge Auger, Donald Poirier
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     ¦Â-D-glucoside of ¦Á-spinasterol
    ÏàËÆ¶È:51.4%
Acta Pharmaceutica Sinica          2005          Vol 40          994-996
Isolation and structure identification of the chemical constituents from Gypsophila oldhamiana
SUN Jing-yong ZHONG Ying ZUO Chun-xu YIN Jun-ting WANG Bin
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     benzyl 2¦Â,3¦Á-Dihydroxyurs-12-en-28-oate
C37H54O4     ÏàËÆ¶È:50%
Journal of Natural Products          2008          71(11)          1877-1880
Practical Synthesis of Bredemolic Acid, a Natural Inhibitor of Glycogen Phosphorylase
Keguang Cheng, Pu Zhang, Jun Liu, Juan Xie, and Hongbin Sun
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     gilvsin B
C31H50O4     ÏàËÆ¶È:50%
Phytochemistry          2009          70          558-563
Lanostane-triterpenoids from the fungus Phellinus gilvus
Hui-Kang Liu, Tung-Hu Tsai, Tun-Tschu Chang, Cheng-Jen Chou, Lie-Chwen Lin
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     gilvsin D
C30H48O3     ÏàËÆ¶È:50%
Phytochemistry          2009          70          558-563
Lanostane-triterpenoids from the fungus Phellinus gilvus
Hui-Kang Liu, Tung-Hu Tsai, Tun-Tschu Chang, Cheng-Jen Chou, Lie-Chwen Lin
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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