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23.2,23.3,23.4,23.9,26.1,34.5,38.3,45.2,48.8,49.5,50.5,52.1,53.4,60.0,69.5,71.7,102.6,132.9,149.6,169.1,169.2,175.7,201.0,214.4
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1 .     (1R*,2E,4R*,7E,10S*,11S*,12R*)-10,18-diacetoxydolabella-2,7-dien-6-one
C24H36O5     ÏàËÆ¶È:58.3%
Journal of Natural Products          1998          61          1096-1100
Three Dolabellanes and a Macrolide from the Sponge Dysidea sp. from Palau
Qing Lu and D. John Faulkner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     8-Deepoxyangeloyl-8-[2-hydroxy-3-chloro-isobutyroyl]enhydrin
    ÏàËÆ¶È:54.1%
Phytochemistry          1995          38          433-435
2¦Á, 3¦Â-dihydroxy-4(18)-neo-cleroden-15-oic acid from cistus populifolius
Julio G. Urones, Isidro S. Marcos, Pilar Basabe, Alicia Jimenez, Antonio Gomez, Anna M. Lithgow
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     20¦Á-Acetylamino-11¦Á-hydroxy-5¦Á-pregnan-3-on
    ÏàËÆ¶È:54.1%
Steroids          1998          63          484-495
Microbial hydroxylation of acetylaminosteroids
HerbertL Holland, Gingipalli Lakshmaiah, PeterL Ruddock
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     khayanone
C27H34O9     ÏàËÆ¶È:51.8%
Journal of Natural Products          2001          64          1107-1110
Antifeedant Rings B and D Opened Limonoids from Khaya senegalensis
Munehiro Nakatani,Samir A. M. Abdelgaleil,Junichi Kurawaki, Hiroaki Okamura,Tetsuo Iwagawa, and Matsumi Doe
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     khayanone
    ÏàËÆ¶È:51.8%
Natural Product Research          2008          22          763-800
13C NMR spectroscopy of D and B, D-ring seco-limonoids of Meliaceae family
T. Narender; T. Khaliq; Shweta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     compound 6
C27H42N4O7     ÏàËÆ¶È:51.8%
Tetrahedron Letters          2005          46          1483-1487
An efficient entry to new sugar modified ketolide antibiotics
Alex Romero, Chang-Hsing Liang, Yu-Hung Chiu, Sulan Yao, Jonathan Duffield, Steven J. Sucheck, Ken Marby, David Rabuka, Po Yee Leung, Youe-Kong Shue, Yoshi Ichikawa, Chan-Kou Hwang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     longistylumphylline A
C23H29NO3     ÏàËÆ¶È:50%
Helvetica Chimica Acta          2005          Vol. 88          854
Longistylumphyllines A-C, Three New Alkaloids from Daphniphyllum longistylum
Xin Chen, Zha-Jun Zhan, Jian-Min Yue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     terretonin A
C26H32O8     ÏàËÆ¶È:50%
Journal of Natural Products          2005          68          1243-1246
Sesterterpenoids, Terretonins A−D, and an Alkaloid, Asterrelenin, from Aspergillus terreus
Guo-You Li, Bo-Gang Li, Tao Yang, Jian-Hua Yin, Hua-Yi Qi, Guang-Ye Liu, and Guo-Lin Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     decahydrotabersonine
    ÏàËÆ¶È:50%
Journal of Natural Products          1997          60          419-420
Perhydrogenation of Tabersonine, an Aspidosperma Indole Alkaloid
Guy Lewin, Corinne Schaeffer, and Catherine Dacquet
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     Daphlongamine F
C23H29NO4     ÏàËÆ¶È:50%
Helvetica Chimica Acta          2009          92          653-659
Alkaloids from the Leaves of Daphniphyllum lo
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