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Cul/8-Hydroxyquinalidine Promoted N-Arylation of Indole and Azoles 被引量:1

Cul/8-Hydroxyquinalidine Promoted N-Arylation of Indole and Azoles
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摘要 An efficient catalytic system of CuI/8-hydroxyquinalidine was developed for the coupling of aryl iodides and indole as well as some azoles. The reaction could be carried out at 90 ~C under the condition of relatively low cata- lyst loading, affording various N-arylindoles and N-aryl azoles in good yields. The functionalized and hindered aryl iodides were suitable substrates for this transformation. An efficient catalytic system of CuI/8-hydroxyquinalidine was developed for the coupling of aryl iodides and indole as well as some azoles. The reaction could be carried out at 90 ~C under the condition of relatively low cata- lyst loading, affording various N-arylindoles and N-aryl azoles in good yields. The functionalized and hindered aryl iodides were suitable substrates for this transformation.
出处 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2012年第4期875-880,共6页 中国化学(英文版)
关键词 COPPER Ullmann reaction 8-hydroxyquinalidine CROSS-COUPLING INDOLE AZOLES copper, Ullmann reaction, 8-hydroxyquinalidine, cross-coupling, indole, azoles
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