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1 . compound 2 C20H28O4 ÏàËÆ¶È:100% Journal of Natural Products 2012 75 2188-2192 Clerodane Diterpenoids from Croton crassifolius Guo-Cai Wang, Jia-Gui Li, Guo-Qiang Li, Jiao-Jiao Xu, Xia Wu, Wen-Cai Ye, and Yao-Lan Li Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . 9-[2-(2(5H)-furanone-4-yl)ethyl]-4,8,9-trimethyl-1,2,3,4,5,6,7,8-octahydronaphthalene-4-carboxylic acid C20H28O4 ÏàËÆ¶È:95% Journal of Asian Natural Products Research 2012 14 785-788 Two new diterpenoids from Croton crassifolius Ying Hu, Lei Zhang, Xiao-Qiong Wen, Xiao-Jun Zeng, Wen Rui & Ying-Zhou Cen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 9-[2-(2(5H)-furanone-4-yl)ethyl]-4,8,9-trimethyl-1,2,3,4,5,6,7,8-octahydro-naphthalene-4-carboxylic acid C20H28O4 ÏàËÆ¶È:95% Chinese Traditional and Herbal Drugs 2013 44 1231-1236 Chemical constituents of Croton crassifolius ZHU Yao-kui, HU Ying, CHENG Ni, CEN Ying-zhou Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . Methyl 9-[2-(2(5H)-furanone-4-yl)ethyl]-4,8,9-trimethyl-1,2,3,4,5,6,7,8-octahydronaphthalene-4-carboxylic ester C21H30O4 ÏàËÆ¶È:90.4% Journal of Asian Natural Products Research 2012 14 785-788 Two new diterpenoids from Croton crassifolius Ying Hu, Lei Zhang, Xiao-Qiong Wen, Xiao-Jun Zeng, Wen Rui & Ying-Zhou Cen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . compound 1 C21H30O4 ÏàËÆ¶È:90.4% Journal of Natural Products 2012 75 2188-2192 Clerodane Diterpenoids from Croton crassifolius Guo-Cai Wang, Jia-Gui Li, Guo-Qiang Li, Jiao-Jiao Xu, Xia Wu, Wen-Cai Ye, and Yao-Lan Li Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 9-[2-(2(5H)-furanone-4-yl)ethyl]-4,8,9-trimethyl-1,2,3,4,5,6,7,8-octahydronaphthalene-4-carboxylic ester C21H30O4 ÏàËÆ¶È:90.4% Chinese Traditional and Herbal Drugs 2013 44 1231-1236 Chemical constituents of Croton crassifolius ZHU Yao-kui, HU Ying, CHENG Ni, CEN Ying-zhou Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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²éѯ½á¹û£º¹²²éµ½1231¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . compound 2 C20H28O4 ÏàËÆ¶È:100% Journal of Natural Products 2012 75 2188-2192 Clerodane Diterpenoids from Croton crassifolius Guo-Cai Wang, Jia-Gui Li, Guo-Qiang Li, Jiao-Jiao Xu, Xia Wu, Wen-Cai Ye, and Yao-Lan Li Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 9-[2-(2(5H)-furanone-4-yl)ethyl]-4,8,9-trimethyl-1,2,3,4,5,6,7,8-octahydronaphthalene-4-carboxylic acid C20H28O4 ÏàËÆ¶È:95% Journal of Asian Natural Products Research 2012 14 785-788 Two new diterpenoids from Croton crassifolius Ying Hu, Lei Zhang, Xiao-Qiong Wen, Xiao-Jun Zeng, Wen Rui & Ying-Zhou Cen Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 9-[2-(2(5H)-furanone-4-yl)ethyl]-4,8,9-trimethyl-1,2,3,4,5,6,7,8-octahydro-naphthalene-4-carboxylic acid C20H28O4 ÏàËÆ¶È:95% Chinese Traditional and Herbal Drugs 2013 44 1231-1236 Chemical constituents of Croton crassifolius ZHU Yao-kui, HU Ying, CHENG Ni, CEN Ying-zhou Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . Methyl 9-[2-(2(5H)-furanone-4-yl)ethyl]-4,8,9-trimethyl-1,2,3,4,5,6,7,8-octahydronaphthalene-4-carboxylic ester C21H30O4 ÏàËÆ¶È:90.4% Journal of Asian Natural Products Research 2012 14 785-788 Two new diterpenoids from Croton crassifolius Ying Hu, Lei Zhang, Xiao-Qiong Wen, Xiao-Jun Zeng, Wen Rui & Ying-Zhou Cen Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . compound 1 C21H30O4 ÏàËÆ¶È:90.4% Journal of Natural Products 2012 75 2188-2192 Clerodane Diterpenoids from Croton crassifolius Guo-Cai Wang, Jia-Gui Li, Guo-Qiang Li, Jiao-Jiao Xu, Xia Wu, Wen-Cai Ye, and Yao-Lan Li Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 9-[2-(2(5H)-furanone-4-yl)ethyl]-4,8,9-trimethyl-1,2,3,4,5,6,7,8-octahydronaphthalene-4-carboxylic ester C21H30O4 ÏàËÆ¶È:90.4% Chinese Traditional and Herbal Drugs 2013 44 1231-1236 Chemical constituents of Croton crassifolius ZHU Yao-kui, HU Ying, CHENG Ni, CEN Ying-zhou Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . ent-halima-5(10),13-dien-16,15-olide C20H30O2 ÏàËÆ¶È:75% Phytochemistry 1995 38 189-194 Clerodane and ent-halimane diterpenes from polyalthia longifolia Noriyuki Hara, Hitomi Asaki, Yoshinori Fujimoto, Yogesh Kumar Gupta, Ashish Kumar Singh, Mahendra Sahai Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 5(10),13E-ent-halimadien-15,16-olide C20H30O2 ÏàËÆ¶È:75% Tetrahedron Letters 2003 44 369-372 Synthesis and absolute configuration of three natural ent-halimanolides with biological activity I.S Marcos, A.B Pedrero, M.J Sexmero, D Diez, P Basabe, F.A Hern¨¢ndez, J.G Urones Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . amphiacric acid B ÏàËÆ¶È:70% Journal of Natural Products 1996 59 5-14 cis-Clerodane Diterpene Lactones from Amphiachyris dracunculoides. Fathalla M. Harraz, Michael J. Pcolinski, and Raymond W. Doskotch Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . ent-halima-5(10),13E-dien-16-oicacid ÏàËÆ¶È:70% Phytochemistry 1995 38 189-194 Clerodane and ent-halimane diterpenes from polyalthia longifolia Noriyuki Hara, Hitomi Asaki, Yoshinori Fujimoto, Yogesh Kumar Gupta, Ashish Kumar Singh, Mahendra Sahai Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 5-[2-(furan-3-yl)ethyl]-1,5,6-trimethyl-1,2,3,4,5,6,7,8-octahydronaphthalene-1-carboxylic acid C20H28O3 ÏàËÆ¶È:65% Journal of Natural Products 2005 68 7-10 ent-Halimane Diterpenes and a Guaiane Sesquiterpene from Cladogynos orientalis Mayuree Kanlayavattanakul, Nijsiri Ruangrungsi, Toshiko Watanabe, Masatoshi Kawahata, Bruno Therrien, Kentaro Yamaguchi, and Tsutomu Ishikawa Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 5(10),14-halimadien-13-ol C20H34O ÏàËÆ¶È:65% Journal of Natural Products 2001 64 1309-1317 Sesqui- and Diterpenoids from the Japanese Liverwort Jungermannia infusca Fumihiro Nagashima,Makoto Suzuki, Shigeru Takaoka, and Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . crotohalimoneic acid C20H26O4 ÏàËÆ¶È:65% Planta Medica 2004 70 87-89 New Halimane Diterpenoids from Croton oblongifolius Sophon Roengsumran ,Surachai Pornpakaku, Nongnuj Muangsin ,Polkit Sangvanich , Thumnoon Nhujak , Pravit Singtothong,Narongsak Chaichit , Songchan Puthong , Amorn Petsom Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 13,19-dihydroxy-halima-5(10),14-diene C20H34O2 ÏàËÆ¶È:65% Biochemical Systematics and Ecology 2004 32 45-53 Diterpenes from Stevia gilliesii Tamara L. Meragelman, Diego S. Pedrosa, Roberto R. Gil Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . compound 8 C20H30O4 ÏàËÆ¶È:65% Tetrahedron 1986 42 3461-3470 Stereochemistry of cis-clerodane diterpenes Shunichi Manabe, Chikao Nishino Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 5(10),14-ent-halimadien-3¦Â,13S-diol C20H34O2 ÏàËÆ¶È:65% Zeitschrift f¨¹r Naturforschung C 2010 65 39-42 Anticancer Activity of Diterpenoids from Amoora ouangliensis and Amoora stellato-squamosa S.-M. Yang, D.-G. Wu, and X.-K. Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . (1S,3Z,7S,8S,11S,12S)-(+)-7,8-epoxyverticill-3-en-12,20-diol 20-acetate C22H36O4 ÏàËÆ¶È:63.6% Phytochemistry 2008 69 2844-2848 Oxygenated verticillene derivatives from Bursera suntui Hugo A. Garc¨ªa-Guti¨¦rrez, Carlos M. Cerda-Garc¨ªa-Rojas, Juan D. Hern¨¢ndez-Hern¨¢ndez,Luisa U. Rom¨¢n-Mar¨ªn, Pedro Joseph-Nathan Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . methyl 3-keto-grindelate C21H32O4 ÏàËÆ¶È:61.9% Phytochemistry 1991 30 1847-1848 Grindelane derivatives by microbial transformation Adetunji J. Aladesanmi, Joseph J. Hoffmann Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . compound 13 ÏàËÆ¶È:61.9% Magnetic Resonance in Chemistry 1987 25 1087-1090 13C NMR spectra of eudesmanolides. II. Eudesman-12,8-olides J. A. Marco and M. Carda Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 3¦Â,11-dihydroxy-9,11-seco-5¦Á-pregna-11,20-dihydropyran-9-one 3-acetate C23H34O5 ÏàËÆ¶È:60.8% Steroids 2010 75 834-847 Synthesis of cytotoxic novel 9,11-secosterol analogs: Structure/activity studies Boonsong Kongkathip, Anuch Hasakunpaisarn, Suthinee Boonananwong, Ngampong Kongkathip Structure 13C NMR ̼Æ×Ä£Äâͼ |

3Â¥2015-01-13 21:27:44













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