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1 .     4'-O-Methylnorbelladine
    ÏàËÆ¶È:50%
Phytochemistry          1998          49          1037-1047
Biosynthesis of the amaryllidaceae alkaloid Galanthamine
Jörg Eichhorn, Takeshi Takad¦Á, Yasuyuki Kit¦Á, Meinhart H. Zenk
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     compound 15
    ÏàËÆ¶È:50%
Tetrahedron Letters          2001          42          7177-7180
Construction of cis- and trans-octahydroisoquinoline-7-ones via a tandem ring-opening and -closing strategy
David I MaGee, May Ling Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     methyl 2-(2-acetyl-3,5-dihydroxy-4,6-dimethylphenyl)acetate
C13H16O5     ÏàËÆ¶È:50%
Heterocycles          2012          85          413-419
Tumonoic Acids K and L, Novel Metabolites from the Marine-Derived Fungus Penicillium citrinum
Li Chen,* Kai Huang, Ping Zhong, Xiao Hu, Zhe-Xiang Fang, Jiu-lin Wu, and Qi-Qing Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     Z-N-(2,4,6-tri-tert-butylphenyl)propinamide
    ÏàËÆ¶È:50%
Tetrahedron          2013          69          1013-1016
Rotational isomerism in 2,4,6-tri-tert-butylanilides
Nobutaka Ototake, Isao Takahashi, Shiori Tsukagoshi, Tatsuki Maeda, Osamu Kitagawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     1-methyl-2,3-dihydro-4-dimethylamino-1-aza-9-azonia-1H-benz[f]indene perchlorate
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Magnetic Resonance in Chemistry          1986          24          137-144
Condensation of 1,3-trimethinecyanines with arylamines. Structural assignment of the products by NOE difference spectroscopy
G¨¢bor T¨®th, Istv¨¢n Bitter, Glen Bigam and Ott¨® Strausz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     3-Methyl-4-[methyl(phenyl)amino]-4-oxobutyl Cyclopropanecarboxylate
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Helvetica Chimica Acta          2011          94          28-37
Reactions with 4-Hydroxy-2-methylbutananilides: Unexpected Formation of a Cyclopropanecarboxamide
Maged K. G. Mekhael, Anthony Linden and Heinz Heimgartner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     (-)-Cyano Ester
C132H19O2N     ÏàËÆ¶È:50%
Journal of the American Chemical Society          1983          105          7713-7719
Camphorae: chiral intermediates for the enantiospecific total synthesis of steroids. 1
Robert V. Stevens, Fred C. A. Gaeta, David S. Lawrence
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     (5S*,6S*)-threo-5,6-Bis(4-methoxyphenyl)-1-octanol
    ÏàËÆ¶È:50%
Journal of Medicinal Chemistry          1989          32          1538-1547
Hexestrol-linked cytotoxic agents: synthesis and binding affinity for estrogen receptors
Hannelore Koehle, Karsten Krohn, Guy Leclercq
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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