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Volumn 78, Issue 11, 2013, Pages 5700-5704

Copper(I)-catalyzed synthesis of 5-arylindazolo[3,2- b ]quinazolin-7(5 H)-one via ullmann-type reaction

Author keywords

[No Author keywords available]

Indexed keywords

BROMINE COMPOUNDS; CESIUM COMPOUNDS;

EID: 84879297699     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo400420b     Document Type: Article
Times cited : (57)

References (38)
  • 3
    • 84879299100 scopus 로고    scopus 로고
    • Preparation of atropisomers of 2-purinyl-3-tolyl-quinazolinone derivatives as anti-inflammatory and anticancer agents
    • PCT Int. Appl. WO 2010111432 A1 30 Sep
    • Evarts, J. B.; Ulrich, R. G. Preparation of atropisomers of 2-purinyl-3-tolyl-quinazolinone derivatives as anti-inflammatory and anticancer agents. PCT Int. Appl. WO 2010111432 A1 30 Sep 2010
    • (2010)
    • Evarts, J.B.1    Ulrich, R.G.2
  • 4
    • 84892627792 scopus 로고    scopus 로고
    • Chem. Abstr. 2010, 153, 456375.
    • (2010) Chem. Abstr. , vol.153 , pp. 456375
  • 8
    • 84879315031 scopus 로고    scopus 로고
    • Preparation of quinazolinone quinazolinone derivatives useful in treatment of proliferative diseases and cancer
    • PCT Int. Appl. WO 2009002808 A2 31 Dec
    • Liu, J.; Ali, S. M.; Ashwell, M. A.; Ye, P.; Guan, Y.; Ng, S.-C.; Palma, R.; Yohannes, D. Preparation of quinazolinone quinazolinone derivatives useful in treatment of proliferative diseases and cancer. PCT Int. Appl. WO 2009002808 A2 31 Dec 2008
    • (2008)
    • Liu, J.1    Ali, S.M.2    Ashwell, M.A.3    Ye, P.4    Guan, Y.5    Ng, S.-C.6    Palma, R.7    Yohannes, D.8
  • 9
    • 84892627721 scopus 로고    scopus 로고
    • Chem. Abstr. 2009, 150, 98369.
    • (2009) Chem. Abstr. , vol.150 , pp. 98369
  • 14
    • 84879314188 scopus 로고    scopus 로고
    • Preparation of 1 H -indazole derivatives as mineralocorticoid receptor antagonists
    • PCT Int. Appl. WO 2012139495A1 20121018.
    • Lan, P.; Liu, K.; Ogawa, A.; Shen, H.; Yang, C.; Wang, Y.; Beresis, R.; Qi, C. Preparation of 1 H -indazole derivatives as mineralocorticoid receptor antagonists. PCT Int. Appl. 2012, WO 2012139495A1 20121018.
    • (2012)
    • Lan, P.1    Liu, K.2    Ogawa, A.3    Shen, H.4    Yang, C.5    Wang, Y.6    Beresis, R.7    Qi, C.8
  • 15
    • 84879284433 scopus 로고    scopus 로고
    • Preparation of substituted 3-(1 H -benzo[ d ]imidazol-2-yl)-1 H -indazole analogs as inhibitors of the PDK1 kinase for treating proliferative disorders
    • PCT Int. Appl. WO 2012135799 A1 20121004.
    • Bearss, D. J.; Vankayalapati, H.; Sorna, V.; Warner, S. L.; Sharma, S. Preparation of substituted 3-(1 H -benzo[ d ]imidazol-2-yl)-1 H -indazole analogs as inhibitors of the PDK1 kinase for treating proliferative disorders. PCT Int. Appl. 2012, WO 2012135799 A1 20121004.
    • (2012)
    • Bearss, D.J.1    Vankayalapati, H.2    Sorna, V.3    Warner, S.L.4    Sharma, S.5
  • 16
    • 84879300027 scopus 로고    scopus 로고
    • Preparation of salts of indazole derivatives as anticancer agents
    • PCT Int. Appl. WO 2011158931 A1 20111222.
    • Isami, S.; Muramatsu, N.; Tanimura, S. Preparation of salts of indazole derivatives as anticancer agents. PCT Int. Appl. 2011, WO 2011158931 A1 20111222.
    • (2011)
    • Isami, S.1    Muramatsu, N.2    Tanimura, S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.