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zyl812: ½ð±Ò+10, ¡ïÓаïÖú 2013-07-15 09:54:37
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²éѯ½á¹û£º¹²²éµ½215¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     Phosphatidyl-nerol
    ÏàËÆ¶È:60%
Bioorganic & Medicinal Chemistry Letters          2008          18          4044-4046
Synthesis of phosphatidylated-monoterpene alcohols catalyzed by phospholipase D and their antiproliferative effects on human cancer cells
Yukihiro Yamamoto, Masashi Hosokawa, Hideyuki Kurihara, Takashi Maoka, Kazuo Miyashita
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     1-[(11S)-3¦Â-hydroxyeudesma-4,6-dien-12-oyl]-piperidine
C20H31NO2     ÏàËÆ¶È:60%
Tetrahedron          1996          52          10507-10518
Ring-opening aminolysis of sesquiterpene lactones: An easy entry to bioactive sesquiterpene derivatives. Synthesis of (+)-¦Â-cyperone and (−-eudesma-3,5-diene from santonin
Gonzalo Blay, Luz Cardona, Begoña Garc¨ªa, Cristina L. Garc¨ªa, Jos¨¦R. Pedro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     triptinin-A
C21H28O3     ÏàËÆ¶È:57.1%
Phytochemistry          1997          44          1511-1514
Triptinins A and B, two leukotriene D4 antagonistic 19(4¡ú3)-abeo-abietanes from Tripterygium wilfordii
Jingya Xu, Tetsuro Ikekawa, Masanori Ohkawa, Itsuro Yokota, Noriyuki Hara, Yoshinori Fujimoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     viscida-3,9,14-triene
    ÏàËÆ¶È:55%
Phytochemistry          2005          66          941-949
Composition of the essential oil of the liverwort Radula perrottetii of Japanese origin
Hailemichael Tesso, Wilfried A. König, Yoshinori Asakawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     eiseniachloride C
C20H29ClO3     ÏàËÆ¶È:55%
Journal of Natural Products          2003          66          1318-1323
Novel Oxylipin Metabolites from the Brown Alga Eisenia bicyclis
Kenji Kousaka, Nobuyuki Ogi, Yasutomo Akazawa,Makiko Fujieda, Yuzo Yamamoto, Yuuki Takada, and Junji Kimura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     acalycixeniolide F
C20H30O3     ÏàËÆ¶È:55%
Journal of Natural Products          2000          63          254-257
New Xenicane Diterpenoids from the Gorgonian Acalycigorgia inermis
Jung-Rae Rho, Hyi-Seung Lee, Youngwan Seo, Ki Woong Cho, and Jongheon Shin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     (2E,4E,8Z,11E)-2'-hydroxy-N-isobutyl-2,4,8,11-tetradecatetraenamide
C18H29NO2     ÏàËÆ¶È:55%
Chemical & Pharmaceutical Bulletin          1988          36          2362-2365
Amides from Huajiao, Pericarps of Zanthoxylum bungeanum MAXIM.
KENJI MIZUTANI,YUICHIRO FUKUNAGA,OSAMU TANAKA,NAOYUKI TAKASUGI,YUH-ICHIROU SARUWATARI,TOHRU FUWA,TATSUO YAMAUCHI,JIAN WANG,MING-RU JIA,FANG-YAO LI and YI-KUI LING
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     compound 11
    ÏàËÆ¶È:55%
Chemistry of Natural Compounds          1988          24          241-246
1H and 13C NMR SPECTRA OF BIOLOGICALLY ACTIVE COMPOUNDS.III. DIASTEREOMERS OF (¡À)-7-THIA- AND 13-THIA-16-ARYLOXY ANALOGS OF II-DEOXYPROSTAGLANDINS OF THE E l SERIES
L. M. Khalluov, A. A. Panasenko E. V. Vasil'eva, N. A. Danilova,Ya. L. Vel'der, and G. A. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     isobungeanool
    ÏàËÆ¶È:55%
Phytochemistry          1997          46          1123-1126
Alkylamides from pericarps of Zanthoxylum bungeanum
Quanbo Xiong, Dawen Shi, Hirofumi Yamamoto, Mizuo Mizuno
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     Bis[(3¦Â-(3,4-dichlorophenyl)-8-methyl-8-azabicyclo[3.2.1]octan-2¦Â-yl)]methyl octanedioate
C38H48Cl4N2O4     ÏàËÆ¶È:55%
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