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25.3, 26.9, 31.0, 37.1, 37.9, 38.2, 53.5, 61.3, 127.9, 128.2, 172.8, 217.6

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ
2Â¥2013-11-28 08:22:58
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