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shooter652: ½ð±Ò+8, ¡ï¡ï¡ïºÜÓаïÖú 2014-06-18 18:44:56
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²éѯ½á¹û£º¹²²éµ½24¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 1¦Â,10¦Â-epoxydesacetoxymatricarin C15H18O4 ÏàËÆ¶È:68.7% Phytochemistry 1989 28 1765-1767 Sesquiterpene lactones from Achillea abrotanoides Milutin Stefanović,Verica Djermanović,Momčilo Gorunvić,Miodrag Djermanović,Slobodan Macura,Slobodan Milosavljević Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 1¦Â,10¦Â-epoxydehydroleucodin ÏàËÆ¶È:56.2% Journal of Natural Products 2002 65 481-486 Dimeric Guaianolides and a Fulvenoguaianolide from Artemisia myriantha Ho-Fai Wong and Geoffrey D. Brown Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 6¦Â-acetoxy-(1¦Á,10¦Â),(4¦Â,5R)-diepoxi-2¦Â-hydroxygermacrane C17H28O5 ÏàËÆ¶È:52.9% The Journal of Organic Chemistry 2005 70 338-341 Enzyme-Catalyzed Rearrangement of a Diepoxy-germacrane Compound into New 7-epi-Eudesmane Derivatives Andr¨¦s Garc¨ªa-Granados, Mar¨ªa C. Guti¨¦rrez, Antonio Mart¨ªnez, and Francisco Rivas Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (11S)-3,3-(Ethylenedioxy) eudesmano-13,6¦Â-diol ÏàËÆ¶È:52.9% Archives of Pharmacal Research 2011 34 191-198 Synthesis of C6-epimer derivatives of diacetoxy acetal derivative of santonin and their inducing effects on HL-60 leukemia cell differentiation Sin Ho Kweon, Keun Tae Kim, Joon Hee Hong, Tae Sung Kim and Bo Gil Choi Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . compound 1(trans) ÏàËÆ¶È:52.9% Magnetic Resonance in Chemistry 1992 30 1186-1195 Stereochemistry¨Cactivity relationships of ACE inhibitors. Conformational studies by 1H and 13C NMR of perindopril and selected stereoisomers J. P. Bouchet, J. P. Volland, M. Laubie, M. Vincent, B. Marchand and N. Platzer Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 17-Hydroxy-16-hydroxyiminobayeran-19-oic acid C21H33NO4 ÏàËÆ¶È:50% Phytochemistry 2008 69 1528-1533 Plant growth regulation activity of steviol and derivatives Br¨¢s Heleno de Oliveira, J¨²lio C¨¦sar Stiirmer, Jos¨¦ D. de Souza Filho,Ricardo Antonio Ayub Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . infuscol B C15H26O ÏàËÆ¶È:50% 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 8 . hydroxyachillin ÏàËÆ¶È:50% Planta Medica 1994 60 228-231 Anti-Inflammatory Activity of Hydroxyachiffin, a Sesquiterpene Lactone from Tanace turn microphyllurn M.J.Abad, P. Bermejo, S. Valverde, and A. Villar Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 2a ÏàËÆ¶È:50% Planta Medica 1991 57 74-76 New Eudesmanolides Related to Torrentm from Artemisia herba-alba subsp. Valentina Juan F. Sanz,and J. Alberto Marco Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 1, 10¦Â-epoxyachillin ÏàËÆ¶È:50% Planta Medica 1988 54 460-461 Sesquiterpene Lactones from Artemisia assoana J. Alberto Marco,O. Barber¨¢, V. Martinez, D. Strack,and B. Meurer Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 8¦Á-hydroxy-4¦Á, 5¦Á-epoxytaurin C15H20O5 ÏàËÆ¶È:50% Planta Medica 1988 54 447-449 Eudesmanolides from Artemisia santonicum A.H.Mericli, J.Jakupovict F. Bohlmann, B. Damadyan, N. Ozhatay, and B. cubukcu Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 1,10¦Â-epoxyachillin C15H18O4 ÏàËÆ¶È:50% Journal of Natural Products 1989 Vol 52 547 The Stereochemistry and Solid State Conformation of 1,10¦Â-Epoxyachillin J. Alberto Marco, Oscar Barbera, Johann Lex, P. de Clercq, A. de Bruyn Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . compound 15 C16H24O11S ÏàËÆ¶È:50% Canadian Journal of Chemistry 2009 87 1733-1737 A facile method for the preparation of sugar orthoesters promoted by anhydrous sodium bicarbonate Shanqiao Wei, Jinzhong Zhao, and Huawu Shao Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . plenolin ÏàËÆ¶È:50% Phytochemistry 1990 29 2273-2276 Inositol derivatives and pseudoguaianolides from Hymenoxys texana Feng Gao,Huiping Wang,Tom J. Mabry Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . [(1S,2S,5S)-5-(Acetyloxy)cyclohex-3-ene-1,2-diyl]dimethanediyl Diacetate C14H20O6 ÏàËÆ¶È:50% Helvetica Chimica Acta 2010 93 1882-1893 Enzyme-Catalyzed Stereoselective Synthesis of Two Novel Carbasugar Derivatives Ayşeg¨¹l G¨¹m¨¹ş and Cihangir Tanyeli Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . (− -9¦Á-hydroxy-7,11-didehydromatrine C15H22N2O2 ÏàËÆ¶È:50% Fitoterapia 2010 81 524-527 Alkaloids from Sophora flavescens Aition Xiu-Jin Liu, Mei-Ai Cao, Wen-Hai Li, Cheng-Shuo Shen, Shi-Qiang Yan, Cheng-Shan Yuan Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . compound 12 ÏàËÆ¶È:50% Journal of the Chemical Society, Perkin Transactions 1 1993 239-247 Total synthesis of three eudesman-12,8-olides, (¡À)-isoalantolactone, (¡À)-dihydrocallitrisin and (¡À)-septuplinolide; structure revision of septuplinolide Masahiro Tada, Hirokazu Yamada, Akira Kanamori and Kazuhiro Chiba Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . philippinlin B C15H24O2 ÏàËÆ¶È:50% Marine Drugs 2013 11 3735-3741 Oxygenated Ylangene-Derived Sesquiterpenoids from the Soft Coral Lemnalia philippinensis Yun-Jie Xio, Jui-Hsin Su, Bo-Wei Chen, Yen-Ju Tseng, Yang-Chang Wu and Jyh-Horng Sheu Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 11¦Â,13-dihydro-8¦Á-hydroxy-goyazensanolide C15H18O5 ÏàËÆ¶È:50% Journal of the Brazilian Chemical Society 2005 16 677-680 Sesquiterpene Lactones from Minasia alpestris Antônio Eduardo M. Crotti, Wilson R. Cunha, Norberto P. Lopes and João Luis C. Lopes Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . Diaporol I C15H26O3 ÏàËÆ¶È:50% Journal of Natural Products 2012 75 1744-1749 Sesquiterpenoids from the Mangrove-Derived Endophytic Fungus Diaporthe sp. Le Yun Zang, Wei Wei, Ye Guo, Ting Wang, Rui Hua Jiao, Seik Weng Ng, Ren Xiang Tan, and Hui Ming Ge Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . Pivaloyloxymethyl 1,1-dioxide-6-¦Â-[succinimidyloxycarbonylmethylsulfonamido]-penicillinate ÏàËÆ¶È:50% Tetrahedron 2012 68 10818-10826 6-Aminopenicillanic acid (6-APA) derivatives equipped with anchoring arms Annaïck Favre, J¨¦rôme Grugier, Alain Brans, Bernard Joris, Jacqueline Marchand-Brynaert Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . (1R,2R,4S)-Essigsaure-(1,2-epoxy-4-pivaloyloxy-2,6,6-trimethylcyclohexan-1-methyl)ester ÏàËÆ¶È:50% Helvetica Chimica Acta 1988 71 931-956 Synthese von enantiomerenreinen Violaxanthinen und verwandten Verbindungen Murat Acemoglu, Peter Uebelhart, Max Rey and Conrad Hans Eugster Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . (1R,2R,4R)-Essigsaure-(1,2-epoxy-4-pivaloyloxy-2,6,6-trimethylcyclohexan-1-methyl)ester ÏàËÆ¶È:50% Helvetica Chimica Acta 1988 71 931-956 Synthese von enantiomerenreinen Violaxanthinen und verwandten Verbindungen Murat Acemoglu, Peter Uebelhart, Max Rey and Conrad Hans Eugster Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . dehydrotetrahydrohelenalin ÏàËÆ¶È:50% Magnetic Resonance in Chemistry 1987 25 201-202 Carbon-13 NMR spectra of some pseudoguaianolides Guillermo Delgado, Laura Alvarez, Eduardo Huerta, Alfonso Romo de Vivar and Rachel Mata Structure 13C NMR ̼Æ×Ä£Äâͼ |

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