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yjl2007

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30.7, 57.8, 110.9, 116.4, 116.7, 118.9, 121.9, 122.4, 124.9, 125.2, 125.4, 129.8, 149.3, 153.8, 166.3
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yangyinhe

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yjl2007: ½ð±Ò+20 2015-01-30 21:35:00
1 .     (E)-N-tert-butyl-2-(2-(thiophen-3-yl)vinyl)benzofuran-3-amine
C18H19NOS     ÏàËÆ¶È:68.7%
Tetrahedron          2014          70          3751-3756
Base-mediated intramolecular cyclization of (2-propargyl ether) arylimines: an approach to 3-amino-benzofurans
Rafaela Gai, Tha¨ªs Prochnow, Davi F. Back, Gilson Zeni
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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2 .     2-(2-fluorophenyl)-2H-indazole
    ÏàËÆ¶È:66.6%
Journal of Heterocyclic Chemistry          2009          46          1309-1317
Microwave-assisted Cadogan reaction for the synthesis of 2-aryl-2H-indazoles,2-aryl-1H-benzimidazoles,2-carbonylindoles,carbazole,and phenazine
Evelyn Cuevas Creencia,Masahiro Kosaka,Toshikatsu Muramatsu,Masashi Kobayashi,Tomohiro Iizuka and Takaaki Horaguchi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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3 .     (Z)-1-allyl-3-(phenylimino)indolin-2-one
C17H14N2O     ÏàËÆ¶È:66.6%
Tetrahedron          2012          68          3649-3653
Facile and highly diastereoselective synthesis of 3-aminooxindoles via AgOAc-catalyzed vinylogous Mannich reaction
Yu-Hua Shi, Zheng Wang, Ying Shi, Wei-Ping Deng
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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4 .     2,2'-dithiobis[N-(4-carboxvphenyl)-1-methyl-1H-indole-3-carboxamide]
C34H26N4O6S2     ÏàËÆ¶È:66.6%
Journal of Medicinal Chemistry          1995          38          58-67
Tyrosine Kinase Inhibitors. 4. Structure-Activity Relationships among N- and 3-Substituted 2,2'-Dithiobis(1H-indoles) for in vitro Inhibition of Receptor and Nonreceptor Protein Tyrosine Kinases
Brian D. Palmer, Gordon W. Rewcastle, Andrew M. Thompson, Maruta Boyd, H. D. Hollis Showalter, Anthony D. Sercel, David W. Fry, Alan J. Kraker, William A. Denny
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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5 .     N-tert-butyl-2-vinylbenzofuran-3-amine
C14H17NO     ÏàËÆ¶È:66.6%
Tetrahedron          2014          70          3751-3756
Base-mediated intramolecular cyclization of (2-propargyl ether) arylimines: an approach to 3-amino-benzofurans
Rafaela Gai, Tha¨ªs Prochnow, Davi F. Back, Gilson Zeni
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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6 .     6H-Benzofuro[3,2-c][1]benzopyran
    ÏàËÆ¶È:66.6%
Heterocycles          2014          89          2122-2136
One-Pot Preparation of 2-Arylbenzofurans from Oximes with Diaryliodonium Triflate
Kotaro Miyagi, Katsuhiko Moriyama, and Hideo Togo*
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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7 .     6'-bromoindirubin
C16H9O2N2Br     ÏàËÆ¶È:62.5%
Journal of Heterocyclic Chemistry          2009          46          1016-1018
Synthesis of halogenoindirubins
Yasuhiro Tanoue,Yousuke Ikoma,Norihisa Kai and Takeshi Nagai
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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8 .     2-(4-(methylthio)phenyl)-N-(2-pyridinyl)imidazo[1,2-a]pyridin-3-amine
C19H16N4S     ÏàËÆ¶È:62.5%
Bioorganic & Medicinal Chemistry          2009          17          74-84
Discovery of novel analgesic and anti-inflammatory 3-arylamine-imidazo[1,2-a]pyridine symbiotic prototypes
Renata B. Lacerda, Cleverton K.F. de Lima, Leandro L. da Silva, Nelilma C. Romeiro, Ana Luisa P. Miranda, Eliezer J. Barreiro, Carlos A.M. Fraga
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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9 .     3-O-methyl isoamericanoic acid A
C17H16O7     ÏàËÆ¶È:62.5%
Bioorganic & Medicinal Chemistry          2009          17          6414-6421
Anti-tumor-initiating effects of phenolic compounds isolated from the bark of Picea jezoensis var. jezoensis
Shun-ichi Wada, Yumiko Yasui, Harukuni Tokuda, Reiko Tanaka
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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10 .     8-methyl-5,10-dihydroindeno[1,2-b]indole
    ÏàËÆ¶È:62.5%
Journal of Heterocyclic Chemistry          2011          48          1095-1102
One-pot-one-step, microwave-assisted Fischer indole synthesis
Evelyn Cuevas Creencia, Masayuki Tsukamoto and Takaaki Horaguchi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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11 .     N-(2-Fluorophenyl) 8-fluoro-4-hydroxy-2-quinolone-3-carboxamide
C16H10F2N2O3     ÏàËÆ¶È:62.5%
Bioorganic & Medicinal Chemistry          2012          20          7175-7183
N-Phenyl-4-hydroxy-2-quinolone-3-carboxamides as selective inhibitors of mutant H1047R phosphoinositide-3-kinase (PI3K¦Á)
Dima A. Sabbah, Neka A. Simms, Wang Wang, Yuxiang Dong, Edward L. Ezell, Michael G. Brattain, Jonathan L. Vennerstrom, Haizhen A. Zhong
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2Â¥2015-01-27 08:38:37
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