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| 13C NMR (101 MHz) ¦Ä 22.2, 22.5, 29.2, 30.6, 32.1, 35.9, 36.3, 36.3, 37.3, 40.4, 41.2, 45.1, 45.6, 71.3, 73.0 |
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dwblsj: ½ð±Ò+6, ¡ïÓаïÖú 2013-11-19 08:36:24
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dwblsj: ½ð±Ò+6, ¡ïÓаïÖú 2013-11-19 08:36:24
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²éѯ½á¹û£º¹²²éµ½590¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . compound 15 ÏàËÆ¶È:73.3% Phytochemistry 2005 66 249-260 Sesquiterpenes from Cupressus macrocarpa foliage Laurence G. Cool Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 9-O-oxoisocaryolane-1-ol C15H24O2 ÏàËÆ¶È:73.3% Chemical & Pharmaceutical Bulletin 1994 42 941-946 Constituents of Sindora sumatrana MIQ. II. Five New Sesquiterpenoids from the Dried Pods Henry HEYMANN,Yasuhiro TEZUKA,Tohru KIKUCHI and Sutardjo SUPRIYATNA Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . foliachinenol E C15H26O3 ÏàËÆ¶È:73.3% Chemical & Pharmaceutical Bulletin 2011 59(8) 1020-1028 Chemical Structures and Hepatoprotective Effects of Constituents from the Leaves of Salacia chinensis Seikou NAKAMURA,Yi ZHANG,Hisashi MATSUDA, Kiyofumi NINOMIYA, Osamu MURAOKA, and Masayuki YOSHIKAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . compound 16 ÏàËÆ¶È:68.4% Organic Magnetic Resonance 1984 22 736-738 Carbon-13 nuclear magnetic resonance spectra of some heterocyclic D-homoandrostanes Deanna Marcano, Jeannette De M¨¦ndez, Ana C. Ortiz and Mirna Salinas Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (1S,2S,3R,6R,7R)-Epoxy-himachal-7-ol ÏàËÆ¶È:66.6% Molecules 2001 6 M228 (1S, 2S, 3R, 6R, 7R)-Epoxy-himachal-7-ol M. Dakir, E. Lassaba, A. Chekroun and A. Benharref Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Caryolane-1,7¦Á-diol C15H26O2 ÏàËÆ¶È:66.6% Chemical & Pharmaceutical Bulletin 2011 59 1430-1433 Sesquiterpenes from the Secondary Metabolites of Streptomyces sp.(YIM 56130) Zhi YANG, Yabin YANG, Xueqiong YANG, Yong ZHANG, Lixing ZHAO, Lihua XU, and Zhongtao DING Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . Compound 2 ÏàËÆ¶È:66.6% Magnetic Resonance in Chemistry 2005 43 861-863 13C NMR spectral assignment of five epimeric 3-versus 3¦Â-functionalized cholestane pairs S. S. Ramos, L. Santos, P. Almeida, W. B. Motherwell and M. C. Costa Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (4R,8S)-15-hydroxyisocaryolan-9-one C15H24O2 ÏàËÆ¶È:66.6% Journal of Natural Products 2013 76 1016-1024 Phytotoxic Activity and Metabolism of Botrytis cinerea and Structure¨CActivity Relationships of Isocaryolane Derivatives Jociani Ascari, Maria Am¨¦lia Diamantino Boaventura, Jacqueline Aparecida Takahashi, Rosa Dur¨¢n-Patr¨®n, Rosario Hern¨¢ndez-Gal¨¢n, Antonio J. Mac¨ªas-S¨¢nchez, and Isidro G. Collado Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 2a,3a ÏàËÆ¶È:66.6% Journal of Chemical Ecology 2007 33 1421-1429 Byrsonic Acid¡ªthe Clue to Floral Mimicry Involving Oil-Producing Flowers and Oil-Collecting Bees Mariza G. Reis, Aparecida D. de Faria, Isabel Alves dos Santos, Maria do Carmo E. Amaral, Anita J. Marsaioli Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . methyl 3,7-dihydroxy-docosanoate ÏàËÆ¶È:66.6% Journal of Chemical Ecology 2007 33 1421-1429 Byrsonic Acid¡ªthe Clue to Floral Mimicry Involving Oil-Producing Flowers and Oil-Collecting Bees Mariza G. Reis, Aparecida D. de Faria, Isabel Alves dos Santos, Maria do Carmo E. Amaral, Anita J. Marsaioli Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . caryolane-1,6¦Â-Diol C15H26O2 ÏàËÆ¶È:66.6% Acta Pharmaceutica Sinica 2012 47 364-366 Sesquiterpenes and an intermediate 1¦Á,6¦Â,11-eudesmanetriol in the biosynthesis of geosmin from Streptomyces sp. YANG Ya-bin; YANG Zhi; YANG Xue-qiong; ZHANG Yong; ZHAO Li-xing; XU Li-hua; DING Zhong-tao Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 3¦Â-hydroxy-5¦Á-androstane C19H32O ÏàËÆ¶È:63.1% European Journal of Organic Chemistry 2011 4543-4550 Androstanes with Modified Carbon Skeletons Sascha Norden, Matthias Bender, J¨¹rgen Rullkötter and Jens Christoffers Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . androstan-3¦Â-ol ÏàËÆ¶È:63.1% Indian Journal of Chemistry Section B 1986 25B 469-472 Lanthanide-induced Caron-13 NMR Shift Studies on Spirostane Sapogenins P K AGRAWAL & R S THAKUR Structure 13C NMR ̼Æ×Ä£Äâͼ |
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