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Volumn 351, Issue 18, 2009, Pages 3107-3112

Cupric halide-mediated intramolecular halocyclization of N-electron-withdrawing group-substituted 2-alkynylanilines for the synthesis of 3-haloindoles

Author keywords

Alkynes; Copper; Cyclization; Halogenation; Nitrogen heterocycles

Indexed keywords


EID: 73349134009     PISSN: 16154150     EISSN: 15213897     Source Type: Journal    
DOI: 10.1002/adsc.200900609     Document Type: Article
Times cited : (51)

References (70)
  • 10
    • 73349143517 scopus 로고    scopus 로고
    • For representative papers on the synthesis of 3-haloindole mediated by N-halosuccinimides, see:
    • For representative papers on the synthesis of 3-haloindole mediated by N-halosuccinimides, see:
  • 19
    • 73349090145 scopus 로고    scopus 로고
    • For selected papers for the synthesis of 3-haloindoles via other methods, see
    • For selected papers for the synthesis of 3-haloindoles via other methods, see:
  • 27
    • 0038343546 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2003, 42, 2406-2409.
    • (2003) Angew. Chem. Int. Ed , vol.42 , pp. 2406-2409
  • 36
    • 0000646741 scopus 로고    scopus 로고
    • 2-mediated halogenation reactions, see: a C. E. Castro, J. G. Gaughan, D. C. Owsley, J. Org. Chem. 1965, 30, 587-592;
    • 2-mediated halogenation reactions, see: a) C. E. Castro, J. G. Gaughan, D. C. Owsley, J. Org. Chem. 1965, 30, 587-592;
  • 49
    • 0014481664 scopus 로고    scopus 로고
    • 10) has no EPR signal. See: a) D. Cavallini, C. D. Marco, S. Dupre, G. Rotilio, Arch. Biochem. Biophys. 1969, 130, 354-361;
    • 10) has no EPR signal. See: a) D. Cavallini, C. D. Marco, S. Dupre, G. Rotilio, Arch. Biochem. Biophys. 1969, 130, 354-361;
  • 68
    • 0036263378 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2002, 41, 1780-1782.
    • (2002) Angew. Chem. Int. Ed , vol.41 , pp. 1780-1782


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.