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Volumn 71, Issue 2, 1998, Pages 467-473

Palladium-Catalyzed Arylation of Azole Compounds with Aryl Halides in the Presence of Alkali Metal Carbonates and the Use of Copper Iodide in the Reaction

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EID: 0001568295     PISSN: 00092673     EISSN: None     Source Type: Journal    
DOI: 10.1246/bcsj.71.467     Document Type: Article
Times cited : (445)

References (40)
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    • For example: a) R. F. Heck, "Palladium Reagents in Organic Syntheses," Academic Press, New York (1985); b) J. Tsuji, "Palladium Reagents and Catalysts," Wiley, Chichester (1995).
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    • Heck, R.F.1
  • 2
    • 0003441482 scopus 로고
    • Wiley, Chichester
    • For example: a) R. F. Heck, "Palladium Reagents in Organic Syntheses," Academic Press, New York (1985); b) J. Tsuji, "Palladium Reagents and Catalysts," Wiley, Chichester (1995).
    • (1995) Palladium Reagents and Catalysts
    • Tsuji, J.1
  • 8
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    • Reaction of furans, thiophenes or pyrroles with arenes or alkenes using a stoichiometric amount of palladium species: a) Y. Fujiwara, O. Maruyama, M. Yoshidomi, and H. Taniguchi, J. Org. Chem., 46, 851 (1981); b) T. Itahara, J. Org. Chem., 50, 5272 (1985).
    • (1981) J. Org. Chem. , vol.46 , pp. 851
    • Fujiwara, Y.1    Maruyama, O.2    Yoshidomi, M.3    Taniguchi, H.4
  • 9
    • 12344271799 scopus 로고
    • Reaction of furans, thiophenes or pyrroles with arenes or alkenes using a stoichiometric amount of palladium species: a) Y. Fujiwara, O. Maruyama, M. Yoshidomi, and H. Taniguchi, J. Org. Chem., 46, 851 (1981); b) T. Itahara, J. Org. Chem., 50, 5272 (1985).
    • (1985) J. Org. Chem. , vol.50 , pp. 5272
    • Itahara, T.1
  • 14
    • 0000171099 scopus 로고    scopus 로고
    • An efficient carbonylative coupling of 1,2-disubstituted imidazoles with alkenes catalyzed by a ruthenium species has recently been reported, in which initial C-H bond activation at the 4-position of the imidazoles seems to take place selectively and the site is acylated: N. Chatani, T. Fukuyama, F. Kakiuchi, and S. Murai, J. Am. Chem. Soc., 118, 493 (1996).
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 493
    • Chatani, N.1    Fukuyama, T.2    Kakiuchi, F.3    Murai, S.4
  • 18
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    • note
    • 3) since KC1 (2.3 mM) is also sparingly soluble in DMF.
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    • F. Asinger, H. Offermanns, and P. Krings, Leibigs Ann., 719, 145 (1968); Chem. Abstr., 70, 68253k (1969).
    • (1969) Chem. Abstr. , vol.70
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    • E. D. Sytsch, Vkrain. Khim. Zhur., 25, 767 (1958); Chem. Abstr.,54, 13143i (1960).
    • (1960) Chem. Abstr. , vol.54


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.