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youyouma: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, һϾͶԵ½ÁË£¬·Ç³£¸Ðл~ 2013-11-28 14:07:52
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youyouma: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, һϾͶԵ½ÁË£¬·Ç³£¸Ðл~ 2013-11-28 14:07:52
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²éѯ½á¹û£º¹²²éµ½150¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . (-)-Hydroxyjasmonic Acid ÏàËÆ¶È:100% Journal of Agricultural and Food Chemistry 2000 48 235-238 Isolation and Structural Elucidation of Two New Glycosides from Sage (Salvia officinalis L.) Mingfu Wang, Hiroe Kikuzaki, Nanqun Zhu, Sengming Sang, Nobuji Nakatani, and Chi-Tang Ho Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . Methyl (1R,2R,2'Z)-2-(5'-hydroxy-pent-2'-enyl)-3-oxocyclopentaneacetate C13H18O4 ÏàËÆ¶È:84.6% Bioscience, Biotechnology, and Biochemistry 2008 72 2867-2876 Synthesis and Bioactivity of Potassium ¦Â-D-Glucopyranosyl 12-Hydroxy Jasmonate and Related Compounds Yoko NAKAMURA, Ryoji MIYATAKE, Sho INOMATA and Minoru UEDA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . Methyl (1R,2R,2'Z)-2-(5'-hydroxy-pent-2'-enyl)-3-oxocyclopentaneacetate C13H18O4 ÏàËÆ¶È:84.6% Bioscience, Biotechnology, and Biochemistry 2008 72 2867-2876 Synthesis and Bioactivity of Potassium ¦Â-D-Glucopyranosyl 12-Hydroxy Jasmonate and Related Compounds Yoko NAKAMURA, Ryoji MIYATAKE, Sho INOMATA and Minoru UEDA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . (1'R,5'R)-5-(5'-carboxymethyl-2'-oxocyclopentyl)-3Z-pentenyl acetate C14H20O5 ÏàËÆ¶È:64.2% Chemistry of Natural Compounds 2012 48 577-579 A new cyclopentanone derivative from Euphorbia hirta Shao-Ming Chi, Yi Wang, Yan Zhao, Jian-Xin Pu and Xue Du, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . (+)-methyl dihydrojasmonate C13H22O3 ÏàËÆ¶È:61.5% Organic letters 2000 2 2959-2962 Enantioselective Synthesis of Both Enantiomers of Methyl Dihydrojasmonate Using Solid−Liquid Asymmetric Phase-Transfer Catalysis Thierry Perrard, Jean-Christophe Plaquevent, Jean-Roger Desmurs, and Dominique H¨¦brault Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . adamantanethione C31H38SSi ÏàËÆ¶È:61.5% Tetrahedron letters 1983 24 4033-4036 Silathiacyclopropane. Isolation and characterization Wataru Ando, Yoshitaka Hamada, Akira Sekiguchi, Katsuhiko Ueno Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . (-)-jasmonic acid C12H18O3 ÏàËÆ¶È:58.3% Journal of Natural Products 1993 Vol 56 2008 (-)-Jasmonic Acid, a Phytotoxic Substance from Botryodiplodia theobromae: Characterization by NMR Spectroscopic Methods Akhtar Husain, Absar Ahmad, Pawan K. Agrawal Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . compound 3c ÏàËÆ¶È:58.3% Tetrahedron Letters 2001 42 8471-8473 Stereoselective preparation of (E)-¦Å-nitro-¦Â,¦Ã-unsaturated methyl esters: Amberlyst A 27, using microwave, as superior catalyst for the 1,6-conjugate addition of nitroalkanes to methyl 1,3-butadiene-1-carboxylate Roberto Ballini, Giovanna Bosica, Dennis Fiorini Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . compound 3f ÏàËÆ¶È:58.3% Tetrahedron Letters 2001 42 8471-8473 Stereoselective preparation of (E)-¦Å-nitro-¦Â,¦Ã-unsaturated methyl esters: Amberlyst A 27, using microwave, as superior catalyst for the 1,6-conjugate addition of nitroalkanes to methyl 1,3-butadiene-1-carboxylate Roberto Ballini, Giovanna Bosica, Dennis Fiorini Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . compound 9c ÏàËÆ¶È:58.3% Tetrahedron Letters 2002 43 3175-3179 Efficient dehydrocyanation of hindered 1-substituted olefins O. Temmem, D. Uguen, A. De Cian, N. Gruber Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . Dimethyl bis (N-benzyloxycarbonyl)-L-bishomocystine C28H36N2O8S2 ÏàËÆ¶È:58.3% Tetrahedron Letters 2003 44 5251-5253 Utility of tetrathiomolybdate and tetraselenotungstate: efficient synthesis of cystine, selenocystine, and their higher homologues Ramakrishna G. Bhat, Emmanuel Porhiel, Vadivelu Saravanan, Srinivasan Chandrasekaran Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . N-(Cyclohexanemethyl) aspartic acid(monolithium salt) ÏàËÆ¶È:58.3% Tetrahedron Letters 2005 46 2751-2755 Direct synthesis of N-substituted, functionalized aspartic acids using alkali maleates and amines Peter S. Piispanen, Petri M. Pihko Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . Cis-1,4-bis(N¦Á-L-phenylalanine)cyclohexane dicarboxylate C26H30N2O6 ÏàËÆ¶È:58.3% Bioorganic & Medicinal Chemistry 1997 5 2049-2061 The influence of molecular conformation upon the self-assembly of cyclohexane diamide diacids Raymond J. Bergeron, Guo Wei Yao, Gregory W. Erdos, Sam Milstein, Fenglan Gao, Jim Rocca, William R. Weimar, Harry L. Price, Otto Phanstiel IV Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . (¡À) (1S,2S,3R)-2-[(S)-amino(carboxy)methyl]-3-cyclohe-xylcyclopropanecarboxylic acid C12H19O4N1 ÏàËÆ¶È:58.3% Bioorganic & Medicinal Chemistry 2010 18 6089-6098 A new metabotropic glutamate receptor agonist with in vivo anti-allodynic activity Nathan J. Stanley, Mark R. Hutchinson, Trine Kvist, Birgitte Nielsen, Jesper Mosolff Mathiesen, Hans Bräuner-Osborne, Thomas D. Avery, Edward R.T. Tiekink, Daniel Sejer Pedersen, Rodney J. Irvine, Andrew D. Abell, Dennis K. Taylor Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . N-(2-adamantyl)benzamide C17H21NO ÏàËÆ¶È:58.3% Russian Journal of Organic Chemistry 2004 40 497-501 Synthetic Approaches to Physiologically Active Polycyclic Compounds: III. Ritter Reaction with Ketones of the Adamantane and Oxahomoadamantane Series N. V. Averina, G. S. Borisova, O. N. Zefirova, E. V. Selyunina and N. V. Zyk, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ |
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