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1 .     compound 8j
C32H42N2O4     ÏàËÆ¶È:58.6%
Journal of Heterocyclic Chemistry          2007          44          909-914
A facile synthesis of 1-alkyl-5-arylalkoxy-6-methoxy-3,4-dihydroisoquinolines
Heong-Seup Yim,Ho-Kyun Kim,Jeum-Jong Kim,Deok-Heon Kweon,Yong-Jin Yoon,Sang-Gyeong Lee and Jung-Ho Kim
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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2 .     6-epi-avrainvillamide
C26H27N3O4     ÏàËÆ¶È:57.1%
Organic Letters          2013          15          2168-2171
Isolation and Photoinduced Conversion of 6-epi-Stephacidins from Aspergillus taichungensis
Shengxin Cai, Yepeng Luan, Xianglan Kong, Tianjiao Zhu, Qianqun Gu, and Dehai Li
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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3 .     1-Cyclopropyl-7-(4-(4-(5-(2,3-dihydroxybenzamido)-2,2-bis(3-(2,3-dihydroxy benzamido)propyl)pentyloxy)-4-oxobutyl)piperazin-1-yl)-6-fluoro-4-oxo-1,4-dihydro quinoline-3-carboxylic acid
C53H61FN6O14     ÏàËÆ¶È:57.1%
Bioorganic & Medicinal Chemistry          2014          22          4049-4060
Synthesis and antibacterial activity of catecholate¨Cciprofloxacin conjugates
Sylvain Fardeau, Alexandra Dassonville-Klimpt, Nicolas Audic, Andr¨¦ Sasaki, Marine Pillon, Emmanuel Baudrin, Catherine Mulli¨¦, Pascal Sonnet
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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4 .     (4R)-methyl 4-(3-bromo-4-chlorophenyl)-2-hydroxy-5-oxo-3,4,5,6,7,8-hexahydro-2H-chromene-2-carboxylate
C17H16BrClO5     ÏàËÆ¶È:56.2%
Tetrahedron          2014          70          5513-5518
Indium-mediated allenylation of arylacyl bromides in a route for the synthesis of substituted furans
Mei-Huey Lin, Chung-Kai Kuo, Yen-Chih Huang, Yu-Ting Tsai, Chang-Hsien Tsai, Kung-Yu Liang, Yi-Syuan Li, Tsung-Hsun Chuang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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5 .     3¦Â-Acetoxy-17¦Â-(1-p-methoxyphenyl-5-pyrazolyl)androst-5-ene
C31H40N2O3     ÏàËÆ¶È:55.1%
Steroids          2010          75          450-456
Synthesis of regioisomeric 17¦Â-N-phenylpyrazolyl steroid derivatives and their inhibitory effect on 17¦Á-hydroxylase/C17,20-lyase
Zolt¨¢n Iv¨¢nyi, J¨¢nos Wölfling, Tam¨¢s Görbe, Mih¨¢ly Sz¨¦csi, Tibor Wittmann, Gyula Schneider
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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6 .     8-hydroxy-labda-13(16),14-dien-19-yl O-acetyl-cis-coumarate
    ÏàËÆ¶È:54.8%
Phytochemistry          1988          27          2241-2248
Terpenoids from leaves of Juniperus thurifera
A.San Feliciano,M. Medarde,J.L. Lopez,J.M. Miguel del Corral,P. Puebla,A.F. Barrero
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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7 .     compound 2
    ÏàËÆ¶È:54.8%
Tetrahedron Letters          1988          29          6223-6226
The total synthesis of argiotoxins 636, 659 and 673
V.John Jasys, Paul R. Kelbaugh, Deane M. Nason, Douglas Phillips, Nicholas A. Saccomano, Robert A. Volkmann
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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8 .     caseamembrin B
C28H42O7     ÏàËÆ¶È:53.5%
Journal of Natural Products          2004          67          316-321
New Cytotoxic Clerodane Diterpenoids from the Leaves and Twigs of Casearia membranacea
Ya-Ching Shen, Chih-Hsin Wang, Yuan-Bin Cheng, Li-Tung Wang, Jih-Hwa Guh, Ching-Te Chien, and Ashraf Taha Khalil
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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9 .     intrapetacin A
C30H38O8     ÏàËÆ¶È:53.5%
Journal of Natural Products          2001          64          497-501
Bioactive Constituents of the Roots of Licania intrapetiolaris
Nicholas H. Oberlies,Jason P. Burgess, Hern¨¢n A. Navarro,Rosa Elena Pinos, Djaja D. Soejarto,Norman R. Farnsworth, A. Douglas Kinghorn, Mansukh C. Wani, and Monroe E. Wall
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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10 .     Cholest-4¦Á-methyl-7-en-[3,2-c]pyrazole
C29H46N2     ÏàËÆ¶È:53.5%
Steroids          2006          71          476-483
Synthesis and antitumor activity of cholest-4¦Á-methyl-7-en-3¦Â-ol derivatives
Lan He, Yumei Liu, Jiangong Shi, Qiang Pei
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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11 .     3¦Â-Acetoxy-21-chloropregn-5-ene-20¦Â-N-(4-bromophenyl)urethane
    ÏàËÆ¶È:53.5%
Steroids          2008          73          1375-1384
Neighboring group participation: Part 17 Stereoselective synthesis of some steroidal 2-oxazolidones, as novel potential inhibitors of 17¦Á-hydroxylase-C17,20-lyase
D¨®ra Ondr¨¦, J¨¢nos Wölfling, Zolt¨¢n Iv¨¢nyi, Gyula Schneider, Istv¨¢n T¨®th, Mih¨¢ly Sz¨¦csi, J¨¢nos Julesz
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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12 .     8¦Á-hydroxylabda-13(16),14-dien-19-yl (Z )-4-hydroxycinnamate
C29H40O4     ÏàËÆ¶È:53.5%
Phytochemistry          1999          51          793-801
Terpenes and lignans from leaves of Chamaecyparis formosensis
Tung-Chieh Lin, Jim-Min Fang, Yu-Shia Cheng
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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13 .     quassidine D
C28H26N4O3     ÏàËÆ¶È:53.5%
Journal of Natural Products          2010          73          167-171
Quassidines A−D, Bis-¦Â-carboline Alkaloids from the Stems of Picrasma quassioides
Wei-Hua Jiao, Hao Gao, Chen-Yang Li, Feng Zhao, Ren-Wang Jiang, Ying Wang, Guang-Xiong Zhou and Xin-Sheng Yao
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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14 .     riccardin D
    ÏàËÆ¶È:53.5%
Phytochemistry          1994          36          73-76
Chenopodene, marchantin P and riccardin G from the liverwort Marchantia chenopoda
Motoo Tori, Mamiko Aoki, Yoshinori Asakawa
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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15 .     8¦Á-hydroxylabda-13(16),14-dien-19-yl p-methoxycinnamate
C30H42O4     ÏàËÆ¶È:53.5%
Phytochemistry          1994          37          1109-1114
Labdanes from Cryptomeria japonica
Su Wen-Chiung, Fang Jim-Min, Cheng Yu-Shia
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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16 .     16-(4-nitro-benzylidene)-3¦Â-piperidino-5¦Á-androstan-17¦Â-yl acetate
C33H46N2O4     ÏàËÆ¶È:53.5%
Steroids          2011          76          709-723
Synthesis, characterization and biological evaluation of some 16E-arylidene androstane derivatives as potential anticancer agents
Hao Guo, Haotian Wu, Jin Yang, Yuling Xiao, Hans-Josef Altenbach, Guofu Qiu,Hao Hu, Zhongyuan Wu, Xianran He, Dingshan Zhou, Xianming Hu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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17 .     16-(4-nitro-benzylidene)-3¦Â-(4-methylpiperazinyl)-5¦Á-androstan-17¦Â-yl acetate
C33H47N3O4     ÏàËÆ¶È:53.5%
Steroids          2011          76          709-723
Synthesis, characterization and biological evaluation of some 16E-arylidene androstane derivatives as potential anticancer agents
Hao Guo, Haotian Wu, Jin Yang, Yuling Xiao, Hans-Josef Altenbach, Guofu Qiu,Hao Hu, Zhongyuan Wu, Xianran He, Dingshan Zhou, Xianming Hu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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18 .     riccardin D
C28H24O4     ÏàËÆ¶È:53.5%
Phytochemistry          1988          27          2603-2608
Fatty acids and cyclic bis(bibenzyls) from the New Zealand liverwort Monoclea forsteri
Masao Toyota,Fumihiro Nagashima,Yoshinori Asakawa
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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19 .     geodisterol
C28H42O3     ÏàËÆ¶È:53.5%
Tetrahedron Letters          1996          37          8145-8146
Geodisterol, a novel polyoxygenated sterol with an aromatic A ring from the tropical marine sponge Geodia sp.
Gui-Yang-Sheng Wang, Phil Crews
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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20 .     (1R)-1-[3-(Carboxymethoxy)phenyl]-3-(4-methoxyphenyl)-1-propanyl (2S)-1-(3,3-dimethyl-1,2-dioxopentyl)-2-piper-idinecarboxylate
    ÏàËÆ¶È:53.5%
Bioorganic & Medicinal Chemistry          1998          6          1309-1335
Synthesis and activity of bivalent FKBP12 ligands for the regulated dimerization of proteins
Terence Keenan, David R. Yaeger, Nancy L. Courage, Carl T. Rollins, Mary Ellen Pavone, Victor M. Rivera, Wu Yang, Tao Guo, Jane F. Amara, Tim Clackson, Michael Gilman, Dennis A. Holt
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2Â¥2014-11-25 11:22:26
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