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Volumn 352, Issue 18, 2010, Pages 3158-3162

Ligand-free copper-catalyzed amination of heteroaryl halides with alkyl- and arylamines

Author keywords

aminopyridines; aminopyrimidines; copper; ligand free conditions; N heteroarylation

Indexed keywords


EID: 78650339365     PISSN: 16154150     EISSN: 16154169     Source Type: Journal    
DOI: 10.1002/adsc.201000708     Document Type: Article
Times cited : (29)

References (66)
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    • (Eds.: A. R. Katritzky, C. W. Rees), Elsevier, Oxford
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  • 22
    • 78650336598 scopus 로고    scopus 로고
    • For examples in Pd-catalyzed N-heteroarylations of alkyl- and arylamines, see
    • For examples in Pd-catalyzed N-heteroarylations of alkyl- and arylamines, see
  • 39
    • 78650401172 scopus 로고    scopus 로고
    • For reviews, see
    • For reviews, see
  • 59
    • 72149088439 scopus 로고    scopus 로고
    • For ligand-free copper-catalyzed N-heteroarylations of alkylamines, see:,. Only couplings between 3-iodopyridine and 3-bromopyridine were reported in the paper, and the yields remained moderate
    • For ligand-free copper-catalyzed N-heteroarylations of alkylamines, see:, H.-J. Xu, F.-Y. Zheng, Y.-F. Liang, Z.-Y. Cai, Y.-S. Feng, D.-Q. Che, Tetrahedron Lett. 2010, 51, 669. Only couplings between 3-iodopyridine and 3-bromopyridine were reported in the paper, and the yields remained moderate.
    • (2010) Tetrahedron Lett. , vol.51 , pp. 669
    • Xu, H.-J.1    Zheng, F.-Y.2    Liang, Y.-F.3    Cai, Z.-Y.4    Feng, Y.-S.5    Che, D.-Q.6
  • 60
    • 78650395728 scopus 로고    scopus 로고
    • See Supporting Information for details
    • See Supporting Information for details.
  • 61
    • 78650400492 scopus 로고    scopus 로고
    • Previously, CsOAc has been used as base in copper-mediated intra- and intermolecular aminations with (over)stoichiometric quantities of copper salts. For examples, see
    • Previously, CsOAc has been used as base in copper-mediated intra- and intermolecular aminations with (over)stoichiometric quantities of copper salts. For examples, see
  • 64
    • 0347286696 scopus 로고    scopus 로고
    • A catalytic version of this transformation has also been reported, but there only aryl iodides were used as the coupling partners in the intermolecular aminations, see
    • K. Okano, H. Tokuyama, T. Fukuyama, Org. Lett. 2003, 5, 4987. A catalytic version of this transformation has also been reported, but there only aryl iodides were used as the coupling partners in the intermolecular aminations, see
    • (2003) Org. Lett. , vol.5 , pp. 4987
    • Okano, K.1    Tokuyama, H.2    Fukuyama, T.3
  • 66
    • 78650378663 scopus 로고    scopus 로고
    • As a by-product a 17% yield of 3-aminopyridine was obtained
    • As a by-product a 17% yield of 3-aminopyridine was obtained.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.