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xiaoxiao270: ½ð±Ò+4 2013-02-23 09:56:08
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²éѯ½á¹û£º¹²²éµ½887¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . t-cadinol C15H26O ÏàËÆ¶È:100% Planta Medica 1991 57 352-355 T-Cadinol: A Pharmacologically Active Constituent of Scented Myrrh: Introductory Pharmacological Characterization and High Field 1H- and 1C3 -NMR Data Per Claeson, RolfAndersson, and GunnarSamuelsson Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . cadinane T-cadinol ÏàËÆ¶È:100% Phytochemistry 1997 46 1039-1043 Sesquiterpenoids from Pallenis spinosa Giovanni Appendino, Jasmin Jakupovic, Sven Jakupovic Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (+)-T-Cadinol ÏàËÆ¶È:100% Phytochemistry 1993 34 441-444 Mono and sesquiterpenoids from Satureja gilliesii Cecilia Labbe, Mariano Castillo, Joseph D. Connolly Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . compound 4 ÏàËÆ¶È:100% Phytochemistry 1989 28 2717-2721 Sesquiterpenoids and phenolics of Pulicaria paludosa Arturo San Feliciano,Manuel Medarde,Marina Gordaliza,Esther Del Olmo,Jos¨¦ M. Miguel del Corral Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . euparin ÏàËÆ¶È:100% Phytochemistry 1983 22 1457-1459 Sesquiterpene alcohols and triterpenoids from Liatris microcephala Werner Herz, Kinzo Watanabe Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . t-cadinol ÏàËÆ¶È:100% Journal of Ethnopharmacology 2010 132 280-285 Hydrophobic constituents and their potential anticancer activities from Devil's Club (Oplopanax horridus Miq.) Original Research Article Shi Sun, Guang-Jian Du, Lian-Wen Qi, Stainley Williams, Chong-Zhi Wang, Chun-Su Yuan Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . T-cadinol C15H26O ÏàËÆ¶È:93.7% Journal of Agricultural and Food Chemistry 2012 60 124-128 Phytochemicals from Cunninghamia konishii Hayata Act as Antifungal Agents Sen-Sung Cheng, Min-Jay Chung, Chun-Ya Lin, Ya-Nan Wang, and Shang-Tzen Chang Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (1R,4R,4aS,8aS)-1-isocyano-4-isopropyl-1,6-dimethyl-1,2,3,4,4a,7,8,8a-octahydronaphthalene C16H25N ÏàËÆ¶È:81.2% The Journal of Organic Chemistry 2011 76 6558-6573 Total Synthesis of 10-Isocyano-4-cadinene and Its Stereoisomers and Evaluations of Antifouling Activities Keisuke Nishikawa, Hiroshi Nakahara, Yousuke Shirokura, Yasuyuki Nogata, Erina Yoshimura,Taiki Umezawa, Tatsufumi Okino, and Fuyuhiko Matsuda Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . (-)-7-epi-Isojunenol C15H26O ÏàËÆ¶È:73.3% Phytochemistry 1999 52 1519-1524 (-)-7-epi-Isojunenol and (+)-7-epi-junenol, constituents of the liverwort Tritomaria uinquedentata Ute Warmers, Wilfried A. König Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . (¡À)-[1S-(1¦Â,4¦Â,4a¦Â,6¦Á,8a¦Á)]-1,6-Dimethyl-4-(1-methylethyl)-1,2,3,4,4a,5,6,7,8,8a-decahydro-1,6-naphthalenediol ÏàËÆ¶È:73.3% Phytochemistry 1996 42 1097-1103 Three new oxygenated cadinanes from Baccharis species Carmen L. Queiroga, Vera L. Ferracini, A. J. Marsaioli Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . comopund 11 ÏàËÆ¶È:73.3% Phytochemistry 1989 28 2717-2721 Sesquiterpenoids and phenolics of Pulicaria paludosa Arturo San Feliciano,Manuel Medarde,Marina Gordaliza,Esther Del Olmo,Jos¨¦ M. Miguel del Corral Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . ¦Á-cadinol ÏàËÆ¶È:73.3% Phytochemistry 1983 22 1457-1459 Sesquiterpene alcohols and triterpenoids from Liatris microcephala Werner Herz, Kinzo Watanabe Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . (+)-T-cadinol ÏàËÆ¶È:73.3% Chinese Journal of Natural Medicines 2010 8 405-410 Terpenoids from Stems and Leaves of Cupressus gigantea LIU Chun-Mei; ZHOU Hui-Bin; ZHANG Wei-Dong Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 10-isothiocyanato-4-cadinene C16H25NS ÏàËÆ¶È:73.3% Tetrahedron 2000 56 3071-3076 New Isocyano and Isothiocyanato Terpene Metabolites from the Tropical Marine Sponge Acanthella cavernosa Richard J. Clark, Bronwin L. Stapleton, Mary J. Garson Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . ¦Á-cadinol ÏàËÆ¶È:73.3% Journal of the Chinese Chemical Society 2000 47 555-560 The Chemical Constituents from the Heartwood of Eucalyptus citriodora Ching-Kuo Lee* and Ming-Huey Chang Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . (1S,6S,7R,10S)-10-Isothiocyanato-4-cadinene C16H25NS ÏàËÆ¶È:73.3% Journal of Natural Products 2012 75 2232-2235 Confirmation of the Configuration of 10-Isothiocyanato-4-cadinene Diastereomers through Synthesis Keisuke Nishikawa, Taiki Umezawa, Mary J. Garson, and Fuyuhiko Matsuda Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . (1S,6S,7R,10R)-10-epi-10-Isothiocyanato-4-cadinene C16H25NS ÏàËÆ¶È:73.3% Journal of Natural Products 2012 75 2232-2235 Confirmation of the Configuration of 10-Isothiocyanato-4-cadinene Diastereomers through Synthesis Keisuke Nishikawa, Taiki Umezawa, Mary J. Garson, and Fuyuhiko Matsuda Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . lycoposerramine-G C16H25NO3 ÏàËÆ¶È:68.7% Chemical & Pharmaceutical Bulletin 2003 51(10) 1163-1169 Ten New Lycopodium Alkaloids Having the Lycopodane Skeleton Isolated from Lycopodium serratum THUNB. Hiromitsu TAKAYAMA,Kazuaki KATAKAWA,Mariko KITAJIMA, Kentaro YAMAGUCHI,and Norio AIMI Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . (1S,4R,4aS,8aS)-1,2,3,4,4a,7,8,8a-Octahydro-1-isocyano-4-isopropyl-1,6-dimethylnaphthalene (10-Isocyano-4-cadinene) C16H25N ÏàËÆ¶È:68.7% Organic Letters 2010 Vol.12,No.5 904-907 Total Synthesis of 10-Isocyano-4-cadinene and Determination of Its Absolute Configuration Keisuke Nishikawa, Hiroshi Nakahara, Yousuke Shirokura, Yasuyuki Nogata,Erina Yoshimura, Taiki Umezawa, Tatsufumi Okino, and Fuyuhiko Matsuda Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . Isonitrile (10-Isocyano-4-cadinene) C16H25N ÏàËÆ¶È:68.7% The Journal of Organic Chemistry 2011 76 6558-6573 Total Synthesis of 10-Isocyano-4-cadinene and Its Stereoisomers and Evaluations of Antifouling Activities Keisuke Nishikawa, Hiroshi Nakahara, Yousuke Shirokura, Yasuyuki Nogata, Erina Yoshimura,Taiki Umezawa, Tatsufumi Okino, and Fuyuhiko Matsuda Structure 13C NMR ̼Æ×Ä£Äâͼ |
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