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Â½ÔÆ´«Ææ: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-10-30 22:19:34
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Â½ÔÆ´«Ææ: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-10-30 22:19:34
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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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |
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