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1 .     5-Hydroxy-4'-chloroflavone
    ÏàËÆ¶È:68.7%
Bulletin of the Korean Chemical Society          2005          26          1461-1463
A Novel Synthesis of Flavones from 2-Methoxybenzoic Acids
Jae In Lee*, Hwa Soo Son, Mi Gung Jung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     5-hydroxyflavone
    ÏàËÆ¶È:62.5%
Chemistry of Natural Compounds          1977          13          429-434
13C NMR SPECTRA OF 3- AND 5-SUBSTITUTED FLAVONE DERIVATIVES
G. A. Kaiabin, N. N. Pogodaeva,N. A. Tyukavklna, and D. F. Kushnarev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     5-Hydroxyflavone
    ÏàËÆ¶È:62.5%
Journal of Natural Products          1990          Vol 53          1471
Microbiological Transformation of Chromone, Chromanone, and Ring A Hydroxyflavones
Abdel-Rahim Ibrahim, Yusuf J. Abul-Hajj
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     5-Hydroxyflavone
    ÏàËÆ¶È:62.5%
Journal of Natural Products          1990          Vol 53          1471
Microbiological Transformation of Chromone, Chromanone, and Ring A Hydroxyflavones
Abdel-Rahim Ibrahim, Yusuf J. Abul-Hajj
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     4'-chloro-¦Á,¦Â-epoxy-5-hydroxy-2-styrylchromone
C17H11ClO4     ÏàËÆ¶È:62.5%
Journal of Heterocyclic Chemistry          2006          43          1319-1326
Epoxidation studies of 2-styrylchromones using jacobsen's catalyst and hydrogen peroxide and iodosylbenzene as oxidants
Clementina M. M. Santos,Artur M. S. Silva,Jos¨¦ A. S. Cavaleiro,Tam¨¢s Patonay and Albert L¨¦vai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     ¦Á,¦Â-epoxy-5-hydroxy-4'-nitro-2-styrylchromone
C17H11NO6     ÏàËÆ¶È:62.5%
Journal of Heterocyclic Chemistry          2006          43          1319-1326
Epoxidation studies of 2-styrylchromones using jacobsen's catalyst and hydrogen peroxide and iodosylbenzene as oxidants
Clementina M. M. Santos,Artur M. S. Silva,Jos¨¦ A. S. Cavaleiro,Tam¨¢s Patonay and Albert L¨¦vai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     primuletin
    ÏàËÆ¶È:62.5%
Magnetic Resonance in Chemistry          2009          47          1043-1054
NMR of a series of novel hydroxyflavothiones (pages 1043¨C1054)
Tuyen Kim Pham Nguyen, Kim Phi Phung Nguyen, Fadhil S. Kamounah, Wei Zhang and Poul Erik Hansen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     primuletin
    ÏàËÆ¶È:62.5%
Magnetic Resonance in Chemistry          2007          45          674-679
1H and 13C-NMR data of hydroxyflavone derivatives (pages 674¨C679)
Younghee Park, Byoung-Ho Moon, Eunjung Lee, Youngshim Lee, Youngdae Yoon, Joong-Hoon Ahn and Yoongho Lim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     5,4'-Dihydroxyflavone
    ÏàËÆ¶È:62.5%
Magnetic Resonance in Chemistry          2007          45          674-679
1H and 13C-NMR data of hydroxyflavone derivatives (pages 674¨C679)
Younghee Park, Byoung-Ho Moon, Eunjung Lee, Youngshim Lee, Youngdae Yoon, Joong-Hoon Ahn and Yoongho Lim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     5-hydroxyflavone
    ÏàËÆ¶È:62.5%
Magnetic Resonance in Chemistry          2007          45          835-845
A predictive tool for assessing 13C NMR chemical shifts of flavonoids (pages 835¨C845)
Darcy C. Burns, David A. Ellis and Raymond E. March
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     1-(indolyl-2-carbonyl)-4-(2-cyanophenyl)piperazine
C20H18N4O     ÏàËÆ¶È:61.1%
Journal of Medicinal Chemistry          1994          37          999-1014
Discovery, Synthesis, and Bioactivity of Bis(heteroaryl)piperazines. 1. A Novel Class of Non-Nucleoside HIV-1 Reverse Transcriptase Inhibitors
Donna L. Romero, Raymond A. Morge, Carolyn Biles, Norman Berrios-Pena, Paul D. May, John R. Palmer, Paul D. Johnson, Herman W. Smith, Mariano Busso, et. al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     4-(1-benzyl-1H-indol-3-yl)-2-pyrimidinamine
C19H16N4     ÏàËÆ¶È:58.8%
Journal of Heterocyclic Chemistry          2007          44          793-801
Dimethylformamide dimethyl acetal in heterocyclic synthesis: Synthesis of polyfunctionally substituted pyridine derivatives as precursors to bicycles and polycycles
Fathi A. Abu-Shanab,A. M. Hessen and S. A. S. Mousa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     6-ÒìÎìÏ©»ùÇÛ²ËËØ
    ÏàËÆ¶È:58.8%
China Journal of Chinese Materia Medica          2012          37          3734-3737
Chemical constituents from cell suspension cultures of Cudrania tricuspidata
YIN Yun-ze; WANG Rui-shan; CHEN Ri-dao; QIAO Li-rui; YANG Lin; WANG Chun-mei; DAI Jun-gui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     4,7-dimethoxy-1,2,5-trihydroxyphenanthrene
C32H28O10     ÏàËÆ¶È:56.2%
Phytochemistry          2008          69          2627-2633
Non-cannabinoid constituents from a high potency Cannabis sativa variety
Mohamed M. Radwan, Mahmoud A. ElSohly, Desmond Slade, Safwat A. Ahmed, Lisa Wilson,Abir T. El-Alfy, Ikhlas A. Khan, Samir A. Ross
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     5-hydroxy-2-(2-phenylethyl)chromone
C17H14O3     ÏàËÆ¶È:56.2%
Journal of Natural Products          2006          69(2)          290-291
Neuroprotective 2-(2-Phenylethyl)chromones of Imperata cylindrica
Jeong Seon Yoon, Mi Kyeong Lee, Sang Hyun Sung, and Young Choong Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     denbinobin
    ÏàËÆ¶È:56.2%
Journal of Natural Products          2001          64          1084-1086
Two Phenanthraquinones from Dendrobium moniliforme
Tzong-Huei Lin, Shu-Jen Chang,Chung-Chuan Chen,Jih-Pyang Wang,and Lo-Ti Tsao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     denbinobin
    ÏàËÆ¶È:56.2%
Journal of Natural Products          1999          62          1225-1227
Antioxidant Principles from Ephemerantha lonchophylla
Hon-Yi Chen, Ming-Shi Shiao, Yu-Lin Huang, Chien-Chang Shen, Yun-Lian Lin, Yueh-Hsiung Kuo, and Chien-Chih Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     ephedroidin
C20H18O6     ÏàËÆ¶È:56.2%
Journal of Natural Products          1998          61          1404-1406
Flavonoids from Genista ephedroides
Luisa Pistelli, Alessandra Bertoli, Isa Giachi, and Antonio Manunta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     auxenone
C16H12O6     ÏàËÆ¶È:56.2%
Phytochemistry          2000          55          793-797
Anthracene derivatives from Auxemma oncocalyx
Walleska B. Marques, H¨¦lcio S. dos Santos, Ot¨ªlia D.L. Pessoa, Raimundo Braz-Filho, Telma L.G. Lemos
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     2-methyl-1,3,6-trihydroxy-9,10-anthraquinone
    ÏàËÆ¶È:56.2%
Chemical & Pharmaceutical Bulletin          1983          31          2353-2358
Studies on a Novel Anthraquinone and Its Glycosides isolated from Rubia cordifolia and R. akane
HIDEJI ITOKAWA,KAZUHIKO MIHARA and KOICHI TAKEYA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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