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gaoaicai123

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22.8,30.7,32.9,44.3,44.4,44.6,44.8,44.9,45.1,45.3,119.7,126.5,127.4,132.6,134.1,136.1,137.1,164.5,172.5
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karl2100: ½ð±Ò+1, лл»Ø¸´£¡ 2013-09-11 22:17:39
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1 .     (-)-ethyl 18-chloro-4,5¦Á-epoxy-3-hydroxy-N-methyl-6¦Á,14¦Á-ethnoisomorphinan-7¦Á-carboxylate
C22H24NO4Cl     ÏàËÆ¶È:59.0%
Recueil des Travaux Chimiques des Pays-Bas          1993          112          113-122
Synthesis and biological activity of new etorphine analogues from 7-chloro-6-demethoxythebaine and 7-chloro-5¦Â-methyl-6-demethoxythebaine (chemistry of opium alkaloids, part XXXVII)
R. H. Woudenberg and L. Maat
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     (-)-4,5¦Á-Epoxy-6-methoxy-17-methyl-7-propylidene-6¦Á,14¦Á-ethenoisomorphinan-3-ol
C22H35NO3     ÏàËÆ¶È:54.5%
Bioorganic & Medicinal Chemistry          1999          7          529-541
chemistry of opium alkaloids. part 44: Synthesis and opioid receptor binding profile of substituted ethenoisomorphinans and ethenomorphinans
Leendert Maat, Richard H. Woudenberg, Gerrit J. Meuzelaar, Joannes T.M. Linders
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     (-)-ethyl 18-chloro-4,5¦Á-epoxy-3-hydroxy-¦Á,¦Á,N-trimethyl-6¦Á,14¦Á-ethnoisomorphinan-7¦Á-methanol hydrochloride
C22H26NO3Cl     ÏàËÆ¶È:54.5%
Recueil des Travaux Chimiques des Pays-Bas          1993          112          113-122
Synthesis and biological activity of new etorphine analogues from 7-chloro-6-demethoxythebaine and 7-chloro-5¦Â-methyl-6-demethoxythebaine (chemistry of opium alkaloids, part XXXVII)
R. H. Woudenberg and L. Maat
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     5-(4-Methoxyphenyl)-N-{[2-thienylmethylene] amino}-bicyclo[2.2.1]heptane-endo-2,endo-3-dicarboximide
C21H20N2O3S     ÏàËÆ¶È:52.6%
Canadian Journal of Chemistry          2010          88          323-330
Heck-type hydroarylations and 1,3-dipolar cycloaddition reactions of new tricyclic hydrazones
Melek Gul and Nuket Ocal
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     2-(4-(Benzyloxy)-3-nitrophenyl)-2-oxoethyl-4-(tertbutoxycarbonylamino)butanoate
C24H28N2O8     ÏàËÆ¶È:52.6%
Canadian Journal of Chemistry          2011          89          364¨C384
p-Hydroxyphenacyl photoremovable protecting groups ¡ª Robust photochemistry despite substituent diversity
Richard S. Givens, Kenneth Stensrud, Peter G. Conrad II, Abraham L. Yousef, Chamani Perera, Sanjeewa N. Senadheera, Dominik Heger, and Jakob Wirz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     N-(3S-N-L-histidinyl-1,2,3,4-tetrahydroisoquinoline-3-carbonyl)-L-histidine
C22H25N7O4     ÏàËÆ¶È:52.6%
Bioorganic & Medicinal Chemistry          2010          18          1536-1554
2, 3-Diamino acid modifying 3S-tetrahydroisoquinoline-3-carboxylic acids: Leading to a class of novel agents with highly unfolded conformation, selective in vitro anti-platelet aggregation and potent in vivo anti-thrombotic activity
Xiaoyi Zhang, Wei Wang, Shenling Cheng, Ming Zhao, Meiqing Zheng, Heng Wei Chang, Jianhui Wu, Shiqi Peng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     methyl N-4-(4-acetoxymethylbenzamidyl)benzyl-4-aminobutanoate
C22H26N2O5     ÏàËÆ¶È:52.6%
Bioorganic & Medicinal Chemistry          2010          18          7291-7301
Design and preparation of sterol mimetics as potential antiparasitics
Federica Gigante, Marcel Kaiser, Reto Brun, Ian H. Gilbert
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     N-(8-dimethylamino-4-(4-methylphenylsulfonamido)-3-nitronaphthalen-1-yl)-N-methylformamide
C21H22N4O5S     ÏàËÆ¶È:52.6%
Tetrahedron          2013          69          1919-1929
¡®Proton sponge¡¯ amides: unusual chemistry and conversion into superbasic 6,7-bis(dimethylamino)perimidines
Valery A. Ozeryanskii, Marina P. Vlasenko, Alexander F. Pozharskii
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     (-)-4,5¦Á-Epoxy-6-methoxy-7,17¦Á-dimethyl-6¦Á,14-ethenoisomorphinan-3-ol
    ÏàËÆ¶È:52.3%
Bioorganic & Medicinal Chemistry          1999          7          529-541
chemistry of opium alkaloids. part 44: Synthesis and opioid receptor binding profile of substituted ethenoisomorphinans and ethenomorphinans
Leendert Maat, Richard H. Woudenberg, Gerrit J. Meuzelaar, Joannes T.M. Linders
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     N-Hydroxy-3-[1-(3-naphthalen-2-yl-propyl)-2-oxo-2,5-dihydro-1H-pyrrol-3-yl]-propionamide
    ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry Letters          2011          21          1218-1221
Structure and property based design, synthesis and biological evaluation of ¦Ã-lactam based HDAC inhibitors
Eunhyun Choi, Chulho Lee, Jung Eun Park, Jeong Jea Seo, Misun Cho, Jong Soon Kang,Hwan Mook Kim, Song-Kyu Park, Kiho Lee, Gyoonhee Han
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     3-(5-3-methyl-5-[(3-methyl-7-5-[2-(4-methylphenyl)-4-oxo-1,3-thia-zolan-3-yl]-1,3,4-thiadiazol-2-ylbenzofuran-5-yl)methyl]benzo-
C43H34N4O4S4     ÏàËÆ¶È:50%
Chemical & Pharmaceutical Bulletin          2010          58          805-810
Synthesis, Nematicidal and Antimicrobial Activity of 3-(5-3-Methyl-5-[(3-methyl-7-5-[2-(aryl)-4-oxo-1,3-thiazolan-3-yl]-1,3,4-thiadiazol-2-ylbenzofuran-5-yl)methyl]benzofuran-7-yl-1,3,4-thiadiazol-2-yl)-2-(aryl)-1,3-thiazolan-4-one
Cherkupally Sanjeeva Reddy, Dasari Chandrashekar Rao, Vookanti Yakub and Adki Nagaraj
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     6¦Á-isovaleryloxy-1-hydroxy-4¦ÁH-1,10-secoeudesma-5(10),11(13)-dien-12,8¦Â-olide
C20H30O5     ÏàËÆ¶È:50%
Tetrahedron          2010          66          9379-9388
New sesquiterpenes from Inula japonica Thunb. with their inhibitory activities against LPS-induced NO production in RAW264.7 macrophages
Jiang-Jiang Qin, Hui-Zi Jin, Jia-Xian Zhu, Jian-Jun Fu, Qi Zeng, Xiang-Rong Cheng, Yan Zhu, Lei Shan, Shou-De Zhang, Yue-Xing Pan, Wei-Dong Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     neodidennilactone
C30H30O3     ÏàËÆ¶È:50%
Tetrahedron          1994          50          7385-7400
Didemnilactones A and B and neodidemnilactone three new fatty acid metabolites isolated from the tunicate Didemnum moseleyi (Herdman)
Haruki Niwa, Masaru Watanabe, Hideaki Inagaki, Kiyoyuki Yamada
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2013-09-11 14:56:32
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