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IMB001½ð³æ (СÓÐÃûÆø)
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| 13C NMR (150 MHz, MeOD) ¦Ä11.4, 11.7, 12.1, 19.2, 25.1, 25.2, 25.5, 34.7, 37.0, 39.4, 41.8, 43.7, 46.0, 49.5, 59.8, 81.4,82.3, 105.0, 129.1, 138.6, 180.0. |
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IMB001: ½ð±Ò+30, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-10-31 09:47:16
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²éѯ½á¹û£º¹²²éµ½45¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . doianoterpene D C20H32O3 ÏàËÆ¶È:57.1% Phytochemistry 2004 65 2071-2076 Kaurane and abietane diterpenoids from Tripterygium doianum (Celastraceae) Naonobu Tanaka, Nobuyuki Ooba, Hongquan Duan, Yoshihisa Takaishi,Yuka Nakanishi, Kenneth Bastow, Kuo-Hsiung Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . viguilenin C20H30O7 ÏàËÆ¶È:57.1% Phytochemistry 1980 19 1795-1797 Viguilenin, a germacranolide from Viguiera linearis Alfonso Romo De Vivar, Eugene Bratoeff, Eliseo Ontiveros, David C. Lankin, Norman S. Bhacca Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . compound 1a ÏàËÆ¶È:54.5% Phytochemistry 1998 47 1141-1144 Diterpenoid alkaloids from Delphinium uncinatum Ayhan Ulubelen, Muhammad Arfan, Ufuk Sönmez, Ali H. Meriçli, Filiz Meriçli Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . compound 3B ÏàËÆ¶È:54.5% The Journal of Organic Chemistry 1981 46 1840-1846 Structures of cuauchichicine, garryfoline, lindheimerine, and ovatine. Chemical correlation of cuauchichicine with (-)-".beta."-dihydrokaurene S. William Pelletier, Naresh V. Mody, Haridutt K. Desai Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . compound 9 ÏàËÆ¶È:52.3% Helvetica Chimica Acta 2006 Vol. 89 1367 Further New Secoatisane Diterpenoids from the Chinese Mangrove Excoecaria agallocha L. Ji-Dong Wang, Zhen-Yu Li, Wen-Sheng Xiang and Yue-Wei Guo Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 16¦Á,17-dihydroxy-ent-atisan-19-al C20H32O3 ÏàËÆ¶È:52.3% Helvetica Chimica Acta 2004 Vol. 87 758 Chemical Constituents from the Pericarp of Trewia nudiflora Zhi-Zhi Du, Hong-Ping He, Bin Wu, Yue-Mao Shen, and Xiao-Jiang Hao Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 2S-hydroperoxy-12R-hydroxyisobromosphaerol C20H32Br2O4 ÏàËÆ¶È:52.3% Journal of Natural Products 2008 71(8) 1386-1392 Brominated Diterpenes with Antibacterial Activity from the Red Alga Sphaerococcus coronopifolius Vangelis Smyrniotopoulos, Constantinos Vagias, M.Mukhlesur Rahman, Simon Gibbons, and Vassilios Roussis Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 2S-hydroperoxy-12S-hydroxyisobromosphaerol ÏàËÆ¶È:52.3% Journal of Natural Products 2008 71(8) 1386-1392 Brominated Diterpenes with Antibacterial Activity from the Red Alga Sphaerococcus coronopifolius Vangelis Smyrniotopoulos, Constantinos Vagias, M.Mukhlesur Rahman, Simon Gibbons, and Vassilios Roussis Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 11 C21H32O5 ÏàËÆ¶È:52.3% Journal of Natural Products 2007 70 758-762 Tricalysiamides A-D, Diterpenoid Alkaloids from Tricalysia dubia Koichi Nishimura,Yukio Hitotsuyanagi, Noriko Sugeta,Haruhiko Fukaya, Yutaka Aoyagi,Tomoyo Hasuda,Takeshi Kinoshita, and Koichi Takeya Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 7,8-epoxy-1,3,11-cembratriene-13R(¦Á),15R(¦Á),16-triol C20H32O4 ÏàËÆ¶È:52.3% Journal of Natural Products 2002 65 1809-1814 Semisynthesis of New Sarcophine Derivatives with Chemopreventive Activity Isamu Katsuyama, Hesham Fahmy,Jordan K. Zjawiony, Sherief I. Khalifa,Raouf W. Kilada,Takao Konoshima, Midori Takasaki, and Harakuni Tokuda Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . (13S)-6¦Â-Methoxy-3¦Á,5-cyclo-13,14-seco-5¦Á-androstane-14,17-dione 17-oxime ÏàËÆ¶È:52.3% Steroids 2004 69 511-514 Reaction of (13S)-13-iodo-6¦Â-methoxy-3¦Á,5-cyclo-13,14-seco-5¦Á-androstane-14,17-dione with hydroxylamine and its application to the synthesis of new 13,14-seco steroids Vladimir A. Khripach, Vladimir N. Zhabinskii, Anna I. Kuchto, Galina P. Fando, Yuliya Y. Zhiburtovich, Alexander S. Lyakhov, Alla A. Govorova, Marinus B. Groen, Jaap van der Louw, Aede de Groot Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . (1R,3aR,7aR)-1-[(1R,4S)-4,5-Di(tertbutyldimethylsilanyloxy)-1,5-dimethylhexyl]-7amethyl-octahydro-1H-inden-4-one C30H60O3Si2 ÏàËÆ¶È:52.3% Steroids 2006 71 529-540 Synthesis of putative metabolites of 1¦Á,25-dihydroxy-2¦Â-(3-hydroxypropoxy)vitamin D3 (ED-71) Yoshiyuki Ono, Hiroyoshi Watanabe, Ikuo Taira, Keisuke Takahashi, Jun Ishihara, Susumi Hatakeyama, Noboru Kubodera Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 10,11-demethoxychippiine ÏàËÆ¶È:52.3% Natural Product Research 1999 13 143-146 Dippinine A, A New Alkaloid of the Chippiinetype From A Malayan Tabernaemontana Toh-Seok Kam; Kooi-Mow Sim Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . triptocallol C21H32O3 ÏàËÆ¶È:52.3% Phytochemistry 1997 45 293-296 A diterpenoid and triterpenes from tissue cultures of Tripterygium wilfordii Kimiko Nakano, Yoshiko Oose, Yuuko Masuda, Hikari Kamada, Yoshihisa Takaishi Structure 13C NMR ̼Æ×Ä£Äâͼ |
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