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zhiyuan0531: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-10-11 22:14:07
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²éѯ½á¹û£º¹²²éµ½224¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . (+)-aphanamol I ÏàËÆ¶È:100% China Journal of Chinese Materia Medica 2009 34 2891-2894 Chemical constituents from Piper longum LIU Wenfeng, JIANG Zhiyong, CHEN Jijun, ZHANG Xuemei, MA Yunbao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . (+)-Aphanamol I C15H24O2 ÏàËÆ¶È:100% The Journal of Organic Chemistry 1992 57 5370-5376 A short enantiospecific route to isodaucane sesquiterpenes from limonene. On the absolute configuration of (+)-aphanamol I and II. Thomas Hansson, Boerje Wickberg Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . compound 6-Me C16H24O3 ÏàËÆ¶È:68.7% Journal of Natural Medicines 2012 66 453-458 Pyrenes and pyrendiones from Uvaria lucida Masataka Moriyasu, Sousuke Takeuchi, Momoyo Ichimaru, Noriyshi Nakatani and Yumi Nishiyama, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . (1R,6S,7R)-(+)-15-Hydroxysclerosporin C15H20O2 ÏàËÆ¶È:66.6% Journal of Natural Products 2010 73 476-478 Hydroxylated Sclerosporin Derivatives from the Marine-Derived Fungus Cadophora malorum Celso Almeida, Ekaterina Eguereva, Stefan Kehraus, Carsten Siering and Gabriele M. König Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . Cosmosoic Acid C15H22O3 ÏàËÆ¶È:66.6% Helvetica Chimica Acta 2010 93 753-756 Two Novel 15(10¡ú1)Abeomuurolane Sesquiterpenes from Cosmos sulphureus Jyh-Horng Wu, Yi-Fu Chang, Yu-Tang Tung, Minoru Tsuzuki, Akira Izuka, Sheng-Yang Wang and Yueh-Hsiung Kuo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . (-)-10-oxo-isodauc-3-en-15-oic acid C15H22O3 ÏàËÆ¶È:66.6% Journal of Natural Medicines 2012 66 453-458 Pyrenes and pyrendiones from Uvaria lucida Masataka Moriyasu, Sousuke Takeuchi, Momoyo Ichimaru, Noriyshi Nakatani and Yumi Nishiyama, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . rac-5-Methyl-1-oxaspiro[2.13]hexadecane ÏàËÆ¶È:62.5% Helvetica Chimica Acta 2012 95 428-447 Exaltone (=Cyclopentadecanone) from Isomuscone (=Cyclohexadecanone), a One-C-Atom Ring-Contraction Methodology via a Stereospecific Favorskii Rearrangement: Regioselective Application to (-)-(R)-Muscone Christian Chapuis, Fabrice Robvieux, Carole Cantatore, Christine Saint-L¨¦ger, and Laurent Maggi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . infuscol C C15H26O3 ÏàËÆ¶È:60% 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 -------------------------------------------------------------------------------- 9 . Sparteine N1-oxidehydrochloride ÏàËÆ¶È:60% Molecules 2008 13 3-10 NMR Spectra of Sparteine N1-oxide and ¦Á-Isosparteine N-oxide Beata Jasiewicz Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . 9¦Â,10¦Â;12,13-Diepoxyttichodiene ÏàËÆ¶È:60% Phytochemistry 1993 32 93-104 Potential inhibitors of trichothecene biosynthesis in Fusarium culmorum: Epoxidation of a trichodiene derivative Andrew R. Hesketh, Linden gledhill, Barrie W. Bycroft, Paul M. Dewick, John Gilbert Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . 3¦Á-hydroxy-9¦Â,10¦Â;12,13- diepoxytrichodiene ÏàËÆ¶È:60% Phytochemistry 1993 32 93-104 Potential inhibitors of trichothecene biosynthesis in Fusarium culmorum: Epoxidation of a trichodiene derivative Andrew R. Hesketh, Linden gledhill, Barrie W. Bycroft, Paul M. Dewick, John Gilbert Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . (1S*,5S*)-5-[(1S*)-1,2,2-trimethylcyclopentyl]bicyclo[3.1.0]hexan-2-one C14H22O ÏàËÆ¶È:60% Indian Journal of Chemistry 2007 46B 805-817 Total synthesis of (¡À)-¦Â-microbiotene,(¡À)-microbiotol,(¡À)-cyclocuparanol and (¡À)-¦Â-cuparenones Srikrishna,A; Ramachary,D B Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . Cosmosaldehyde C15H22O2 ÏàËÆ¶È:60% Helvetica Chimica Acta 2010 93 753-756 Two Novel 15(10¡ú1)Abeomuurolane Sesquiterpenes from Cosmos sulphureus Jyh-Horng Wu, Yi-Fu Chang, Yu-Tang Tung, Minoru Tsuzuki, Akira Izuka, Sheng-Yang Wang and Yueh-Hsiung Kuo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . (+)-lepidozene C15H24 ÏàËÆ¶È:60% Tetrahedron 1990 46 8237-8242 (+)-Lepidozene a new bicyclic sesquiterpene from the gorgonia lophogorgia ruberrima Manuel Norte, Jos¨¦J. fernd́ez, Rafael Gonz¨¦z, Matias L. Rodr¨ªguez, Catalina Ruiz-P¨¦rez, Victor Rodriguez-Romero Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . (5E,9E)-3-n-butyl-5-methylindolizidine ÏàËÆ¶È:60% Tetrahedron 1986 42 3453-3460 Alkaloids from dendrobatid poison frogs: trans-decahydroquinolines and indolizidines T. Tokuyama, N. Nishimori, I.L. Karle, M.W. Edwards, J.W. Daly Structure 13C NMR ̼Æ×Ä£Äâͼ |
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