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chenyayun: ½ð±Ò+8, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл 2015-05-23 16:41:20
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1 . Serofendic acid B C21H35O4S ÏàËÆ¶È:71.4% Tetrahedron Letters 2002 43 3625-3628 Synthesis and absolute configuration of serofendic acids Taro Terauchi, Naoki Asai, Masahiro Yonaga, Toshiaki Kume, Akinori Akaike, Hachiro Sugimoto Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . bromoterpene C20H33BrO ÏàËÆ¶È:70% Journal of Natural Products 2001 64 696-700 New Bromoterpenes from the Red Alga Laurencia luzonensis Masayuki Kuniyoshi,Mong S. Marma, Tatsuo Higa,G¨¦rald Bernardinelli, and Charles W. Jefford Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 15¦Á-hydroxy-ent-kaur-16-en-19-oic acid ÏàËÆ¶È:70% Planta Medica 1993 59 278-279 Kauranoid Diterpenes in Gynoxys oletfolia S. Catalano,P. L. Cioni, A. Menichini, A. B. Bilia, L Morelli, and V. DeFeo Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 16¦Á-(-)-kauran- 19-al-17-oic acid ÏàËÆ¶È:70% Journal of Natural Products 1985 Vol 48 489-490 Terpenoids from Viguiera potosina Feng Gao, Mahmut Miski, Douglas A. Gage, John A. Norris, Tom J. Mabry Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . compound 6a ÏàËÆ¶È:70% Phytochemistry 1983 22 2543-2546 Ent-kauranes and trachylobanes from Helianthus radula Werner Herz, Palianappan Kulanthaivel Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 16¦Á-hydro-17-hydroxy-ent-kauran-19-al ÏàËÆ¶È:70% Journal of the Chinese Chemical Society 2004 51 869-876 Chemical Constituents from Annona glabra Tian-Jye Hsieh, Yang-Chang Wu, Su-Ching Chen,Ching-Shan Huang and Chung-Yi Chen* Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . (16R)-17-hydroxy-ent-kauran-19-al C20H32O2 ÏàËÆ¶È:70% Biochemical Systematics and Ecology 2013 51 4-7 Diterpenoids and acetylenic lipids from Aralia racemosa Jason A. Clement, Matthew J. Flood, Rachel M. Bleich, Timothy J. Willis, Ryan M. Kelly, Jeffrey D. Schmitt Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . Serofendic acid A C21H35O4S ÏàËÆ¶È:66.6% Tetrahedron Letters 2002 43 3625-3628 Synthesis and absolute configuration of serofendic acids Taro Terauchi, Naoki Asai, Masahiro Yonaga, Toshiaki Kume, Akinori Akaike, Hachiro Sugimoto Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . ethyl (5¦Â,8¦Á,9¦Â,10¦Á,13¦Á)-8-ethenyl-13-(hydroxymethyl)-13-methylpodocarpan-15-oate C23H38O3 ÏàËÆ¶È:65.2% Helvetica Chimica Acta 2010 93 2052-2069 Stereoselective Synthesis, Characterization, and Antibacterial Activities of Novel Isosteviol Derivatives with D-Ring Modification Ya Wu, Cong-Jun Liu, Xu Liu, Gui-Fu Dai, Jin-Yu Du and Jing-Chao Tao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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