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luckyÑà×Ó: ½ð±Ò+8, ¡ï¡ï¡ïºÜÓаïÖú, лл 2015-01-07 22:55:47
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luckyÑà×Ó: ½ð±Ò+8, ¡ï¡ï¡ïºÜÓаïÖú, лл 2015-01-07 22:55:47
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²éѯ½á¹û£º¹²²éµ½83¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . (4R,5S,6R,7R,11S)-12-Hydroxy-1(10)-aromadendren-9-one C15H22O2 ÏàËÆ¶È:60% Journal of Natural Products 2004 67 799-805 Isolation of a Library of Aromadendranes from Landolphia dulcis and Its Characterization Using the VolSurf Approach Brian Skole, Flemming S. Jrgensen, Bogdan A. Budnik, Patrick Ekpe, and Jerzy W. Jaroszewski Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . compmound IVa ÏàËÆ¶È:60% Natural Product Research 1997 10 105-109 On Guaiol Oxygenation Products Rudolph Ernst K. Winter; James A. Baker; Binh V. Lam; Andrew G. Breite; Nigam Rath Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 11-hydroxy-valenc-1(10)-en-2-one C15H24O2 ÏàËÆ¶È:60% Phytochemistry 1987 26 571-572 A valencane sesquiterpenoid from Teucrium carolipaui Giuseppe Savona,Franco Piozzi,Mar¨ªa C. De La Torre,Orietta Servettaz,Benjam¨ªn Rodr¨ªguez Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 11-hydroxyvalenc-1(10)-en-2-one C15H24O2 ÏàËÆ¶È:60% Chemistry of Natural Compounds 2013 49 457-461 Eremophilane-type sesquiterpenes from Alpinia oxyphylla with inhibitory activity against nitric oxide production Junju Xu, Jia Su, Yan Li, Ninghua Tan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 13-hydroxyaromadendr-1(10)-en-9-one C15H22O2 ÏàËÆ¶È:60% Phytochemistry 2001 57 377-383 Biotransformation of squamulosone by Curvularia lunata ATCC 12017 Dwight O Collins, Greg O Buchanan, William F Reynolds, Paul B Reese Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . Inoterpene D pivaloyl ester C35H58O4 ÏàËÆ¶È:57.1% Tetrahedron 2009 65 2443-2450 Absolute stereostructures of inoterpenes A¨CF from sclerotia of Inonotus obliquus Seikou Nakamura, Junko Iwami, Hisashi Matsuda, Shuichi Mizuno, Masayuki Yoshikawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . ¦Á-irone ÏàËÆ¶È:57.1% Molecules 2012 17 2587-2598 New Constituents from the Rhizomes of Egyptian Iris germanica L. Sabrin R. M. Ibrahim, Gamal A. Mohamed and Nawal M. Al-Musayeib Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . 1¦Á,10¦Â,15-trihydroxy-3-oxo-8¦Â-O-methylbutanoyl-4,11(13)-germacradien,6¦Á,12-olide C20H28O8 ÏàËÆ¶È:57.1% Phytochemistry 2001 57 267-272 Sesquiterpene lactones and a myoinositol from glandular trichomes of Viguiera quinqueremis (Heliantheae; Asteraceae) Otmar Spring, Reinhard Zipper, Sabine Reeb, Bernhard Vogler, Fernando B Da Costa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . 1¦Â,7¦Á-dihydroxyleudesman-4-one C14H24O3 ÏàËÆ¶È:57.1% Helvetica Chimica Acta 2014 97 1714-1718 Chemical Constituents of the Leaves of Desmos cochinchinensis var. fulvescens Ban Tung-Ying Wu, Yuan-Bin Cheng, Fu-Ting Cheng, Yu-Ming Hsu, Thang Tran Dinh, Fang-Rong Chang and Yang-Chang Wu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . compound 1 ÏàËÆ¶È:53.8% Phytochemistry 2000 55 749-753 The stereochemistry of ledol from Renealmia chrysotrycha: an NMR study Maria Auxiliadora C. Kaplan, Helena R.L. Pugialli, Daise Lopes, Hugo E. Gottlieb Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . 8¦Á¦Â-methyl-3,4,4a¦Á,5,8,8a-hexahydro 1(2H)-naphthalenone ÏàËÆ¶È:53.8% Natural Product Research 1994 5 165-170 Steroid Synthesis by High Pressure Diels-alder Reaction of 3-methyl-2-cyclopenten-1-one Eszter Gacs-baitz; Assunta Marrocchi; Lucio Minuti; Hans W. Scheeren; Aldo Taticchi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . (E )-7¦ÁH-germacra-1(10),4(15)-diene-5¦Á,6¦Â-diol C15H26O2 ÏàËÆ¶È:53.8% Phytochemistry 1999 51 529-541 Bioactive sesquiterpenes from Santolina rosmarinifolia subsp. Canescens. A conformational analysis of the germacrane ring Alejandro F. Barrero, M. Mar Herrador, Jose F.Quilez, Ramon Alvarez-Manzaneda, Dolores Portal, Jose A. Gavin, Dolores G. Gravalos, M.S.J. Simmonds, W.M. Blaney Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . compound 33 ÏàËÆ¶È:53.8% Indian Journal of Chemistry Section B 2005 44B 751-761 Approaches to sesquiterpenes containing three contiguous quaternary carbon atoms. Synthesis of 3-methoxythapsene Srikrishna,A; Ramachary,D B Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . tert-butyl rel-(3S,5R)-2-oxo-3-[(1Z)-3-(triisopropylsilanyl)propenyl]-5-vinylpyrrolidine-1-carboxylate C23H41NO3Si ÏàËÆ¶È:53.8% Heterocycles 2003 59 573-585 Investigation of the Ring-opening Cross-Metathesis Reaction of 2-Azabicyclo[2.2.1]hept-5-en-3-one (ABH) with Allylsilanes Minoru Ishikura,* Makoto Saijo, and Ayako Hino Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . Compound 4 ÏàËÆ¶È:53.8% Bioorganic & Medicinal Chemistry Letters 2008 18 3043-3046 Synthesis and stereochemistry of the terminal spiroketal domain of the phosphatase inhibitor dinophysistoxin-2 Craig J. Forsyth, Ce Wang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . (-)-4¦Â-hydroxy-¦Â-pinen-6-one C10H14O2 ÏàËÆ¶È:53.8% Zeitschrift f¨¹r Naturforschung C 2002 57 686-690 The Microbial Oxidation of (-)-b-Pinene by Botrytis cinerea A. Farooq, M., I. Choudhary, S. Tahara, Atta-ur-Rahman, K. H. C. Ba\cser, and F. Demirci Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . (2 RS,3S)-3,6-dimethylhept-5-en-2-ol ÏàËÆ¶È:53.8% Journal of Chemical Ecology 2002 28 2541-2555 Identification of New Homoterpene Esters from Dufour's Gland of the Ponerine Ant Gnamptogenys striatula Claudia M. Schulz, Lutz Lehmann, Rumsaïs Blatrix, Pierre Jaisson and Abraham Hefetz, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . exo-N-ethyl(2,2,3-trimethyl-1-norbornyl)amine ÏàËÆ¶È:53.8% Journal of Medicinal Chemistry 1995 38 4474-4477 Synthesis of substituted 1-norbornylamines with antiviral activity. A. Garcia Martinez, E. Teso Vilar, A. Garcia Fraile, S. de la Cerero, M. E. Rodriguez Herrero, P. Martinez Ruiz, L. R. Subramanian, A. Garcia Gancedo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . (2 RS,3S)-3,6-dimethylhept-5-en-2-ol ÏàËÆ¶È:53.8% Journal of Chemical Ecology 2002 28 2541-2555 Identification of New Homoterpene Esters from Dufour's Gland of the Ponerine Ant Gnamptogenys striatula Claudia M. Schulz, Lutz Lehmann, Rumsaïs Blatrix, Pierre Jaisson, Abraham Hefetz, Wittko Francke Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . 3-methyl-2-(4,4,4-trifluoro-3-hydroxybutylamino)-pentanoic acid methyl ester C11H20F3NO3 ÏàËÆ¶È:53.8% Journal of the Brazilian Chemical Society 2005 16 1255-1261 Synthesis of N-Substituted 6-Trifluoromethyl-1,3-oxazinanes Nilo Zanatta, Adriana M. C. Squizani, Leonardo Fantinel, Fabiane M. Nachtigall, Deise M. Borchhardt, Helio G. Bonacorso and Marcos A. P. Martins Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . compound 8i ÏàËÆ¶È:53.8% Australian Journal of Chemistry 1981 34 1451-1465 Carbon-13 N.M.R. studies of 5¦Á- and 5¦Â-Cholestan-5-ols and analogous 8a-Methyl-trans- and cis-decahydronaphthalen-4a-ols JM Coxon and JR Gibson Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . (S)-(p-Menth-1,8-dien-7-ol-7-yl) phosphonic acid,di-tert-butyl ester ÏàËÆ¶È:53.8% Bioorganic & Medicinal Chemistry 1999 7 241-250 Novel limonene phosphonate and farnesyl diphosphate analogues: design, synthesis, and evaluation as potential protein-farnesyl transferase inhibitors Jeffrey T Eummer, Barbara S Gibbs, Todd J Zahn, Judith S Sebolt-Leopold, Richard A Gibbs Structure 13C NMR ̼Æ×Ä£Äâͼ |
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