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Â½ÔÆ´«Ææ: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-10-30 22:19:34
²éѯ½á¹û£º¹²²éµ½31¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     pubescenone
C19H26O3     ÏàËÆ¶È:57.8%
Phytochemistry          2006          67          1708-1715
Structures, biogenetic relationships, and cytotoxicity of pimarane-derived diterpenes from Petalostigma pubescens
Mary H. Grace, Yinghua Jin, George R. Wilson, Robert M. Coates
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     11¦Á,13-dihydroalantolactone
C15H22O2     ÏàËÆ¶È:52.6%
Journal of Natural Products          2001          64          466-471
Sesquiterpenes and Monoterpenes from the Bark of Inula macrophylla
Bao-Ning Su,Yoshihisa Takaishi, Tetsuya Yabuuchi, Takenori Kusumi, Motoo Tori,Shigeru Takaoka,Gisho Honda, Michiho Ito, Yoshio Takeda, Olimjon K. Kodzhimatov, and Ozodbek Ashurmetov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     annosquamosin B
C19H32O3     ÏàËÆ¶È:52.6%
Journal of Natural Products          1996          59          635-637
Identification of ent-16¦Â, 17-Dihydroxykauran-19-oic Acid as an Anti-HIV Principle and Isolation of the New Diterpenoids Annosquamosins A and B from Annona squamosa
Yang-Chang Wu, Yu-Chun Hung, Fang-Rong Chang, Mark Cosentino, Hui-Kang Wang, and Kuo-Hsiung Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     compound 11
    ÏàËÆ¶È:52.6%
Natural Product Research          2009          23          256-263
Hemisynthesis of two marine cheilanthane sesterterpenes from (-)-sclareol: First enantioselective synthesis of petrosaspongiolide R
Leticia Ferreiro-Mederos; Steve Lanners; Hichem Henchiri; Abdelwaheb Fekih; Gilles Hanquet
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     spongi-12-en-11,16-dione
C20H28O3     ÏàËÆ¶È:52.6%
Australian Journal of Chemistry          2011          64          757-765
Structures and Anatomical Distribution of Oxygenated Diterpenes in the Australian Nudibranch Chromodoris reticulata
Suciati, Lynette K. Lambert and Mary J. Garson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     compound 11
C19H28O2     ÏàËÆ¶È:52.6%
Qu¨ªmica Nova          2013          36          778-782
TRACHYLOBANE AND KAURANE DITERPENES FROM Croton floribundus SPRENG.
Paula Karina S. Uchôa, Jos¨¦ Nunes da Silva Jr., Edilberto Rocha Silveira e Mary Anne S. Lima*,Raimundo Braz-Filho,Let¨ªcia Veras Costa-Lotufo, Ana J¨¦rsia Ara¨²jo, Manoel Odorico de Moraes e Claudia do Ó Pessoa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     (1S,2R,4S,4'R)-4'-(1-(tert-Butyldimethylsilyloxy)-3-methylbut-3-enyl)-4',5'-dihydro-2'H-spiro[bicyclo[2.2.1]hept[5]ene-2,3'-furan]-2'-one
C21H34O3Si     ÏàËÆ¶È:52.6%
The Journal of Organic Chemistry          2012          77          6345-6350
Domino Ring-Opening Metathesis¨CRing-Closing Metathesis of Bicyclo[2.2.2]octene Derivatives: Scope and Limitations
Sritama Bose, Manju Ghosh, and Subrata Ghosh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     11,13,17,19-tetrahydrocynaropicrin
C19H26O6     ÏàËÆ¶È:52.6%
Journal of the Science of Food and Agriculture          2005          85          1757-1764
Chemical and biological modification of cynaropicrin and grosheimin: a structure¨Cbitterness relationship study
Giancarlo Cravotto, Gian Mario Nano, Arianna Binello, Paola Spagliardi and Gianfranco Seu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     dendrillol-3
    ÏàËÆ¶È:52.3%
Tetrahedron          1996          52          8187-8198
Dorisenones, cytotoxic spongian diterpenoids, from the nudibranch Chromodoris obsoleta
Tomofumi Miyamoto, Kenichiro Sakamoto, Kazuyoshi Arao, Tetsuya Komori, Ryuichi Higuchi, Takuma Sasaki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2013-10-30 19:27:08
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