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yuncheng6

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11.24,13.99,14.35,19.09,20.82,22.83,23.69,24.9,28.84,30.18,30.44,38.48,64.2,65.45,68.02,91.18,106.61,108.51,109.97,110.00,112.13,119.96,122.02,123.95,129.09,131.95,136.26,140.26,142.25,159.92,164.75,166.54,181.57,188.82

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yuncheng6: ½ð±Ò+5, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-03-29 23:50:29
1 .     Compound 12b
C35H41N2O4     ÏàËÆ¶È:52.9%
Tetrahedron          2001          57          2085-2094
Enantioselective syntheses of coronaridine and 18-methoxycoronaridine
Martin E Kuehne, Timothy E Wilson, Upul K Bandarage, Wenning Dai, Qian Yu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     Compound 12a
C35H41N2O4     ÏàËÆ¶È:51.4%
Tetrahedron          2001          57          2085-2094
Enantioselective syntheses of coronaridine and 18-methoxycoronaridine
Martin E Kuehne, Timothy E Wilson, Upul K Bandarage, Wenning Dai, Qian Yu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     Methyl morellate
C34H38O8     ÏàËÆ¶È:50%
Magnetic Resonance in Chemistry          2007          45          578-582
Guttiferic acid, a novel rearrangement product from minor chromenoxanthone pigments of Garcinia morella Desr. (pages 578¨C582)
D. Rajagopal Rao, K. N. Gurudutt, S. Mamatha and L. J. Mohan Rao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     xylocarpin G
    ÏàËÆ¶È:50%
Chinese Traditional and Herbal Drugs          2009          40          1201-1204
ºìÊ÷ÁÖÖ²Îïľ¹û鬻¯Ñ§³É·ÖµÄÑо¿
ÉòÁ¢Èã;¹ù¶°;Òü±¦Î°;ÕÅÇà;ÕÔÀ×;»ô³¤ºç;ÕÅ‹ Àö;Ê·ÇåÎÄ;ÍõÓÀÀû
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     Trigoxyphin J
C38H58O10     ÏàËÆ¶È:50%
Phytochemistry Letters          2013          6          472-475
Three new terpenoids from Trigonostemon xyphophylloides (Croiz.) L.K. Dai and T.L. Wu
Li Yu, Wen-jian Zuo, Wen-li Mei, Zhi-kai Guo, Xiao-na Li, Hao-fu Dai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     4-[(10-Allyl-9,10-diazatricyclo[4.2.1.1(2,5)]dec-9-yl)-(3-methoxyphenyl)methyl]-N-pyrrolidin-1-yl-benzamide
C30H38N4O2     ÏàËÆ¶È:50%
European Journal of Medicinal Chemistry          2013          69          413-426
Synthesis and biological evaluation of novel delta (¦Ä) opioid receptor ligands with diazatricyclodecane skeletons Original Research Article
Giovanni Loriga, Paolo Lazzari, Stefania Ruiu, Giorgio Marchese, Ilaria Manca, Gian Luca Casu, Christian Dess¨¬, G¨¦rard Aim¨¨ Pinna, Battistina Asproni, Gabriele Murineddu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     4-[(10-Allyl-9,10-diazatricyclo[4.2.1.1(2,5)]dec-9-yl)-(3-hydroxyphenyl)methyl]-N-pyrrolidin-1-yl-benzamide
C29H36N4O2     ÏàËÆ¶È:50%
European Journal of Medicinal Chemistry          2013          69          413-426
Synthesis and biological evaluation of novel delta (¦Ä) opioid receptor ligands with diazatricyclodecane skeletons Original Research Article
Giovanni Loriga, Paolo Lazzari, Stefania Ruiu, Giorgio Marchese, Ilaria Manca, Gian Luca Casu, Christian Dess¨¬, G¨¦rard Aim¨¨ Pinna, Battistina Asproni, Gabriele Murineddu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     1-Methyl-N-(8-((1,2,3,4-tetrahydroacridin-9-yl)amino)octyl)-9H-pyrido[3,4-b]indole-3-carboxamide
C34H39N5O     ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry          2014          22          6089-6104
Design, synthesis and evaluation of novel tacrine-(¦Â-carboline) hybrids as multifunctional agents for the treatment of Alzheimer¡¯s disease
Jin-Shuai Lan, Sai-Sai Xie, Su-Yi Li, Long-Fei Pan, Xiao-Bing Wang, Ling-Yi Kong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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