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Volumn 19, Issue 4, 2013, Pages 1496-1501

Gold(I)-catalyzed aminohalogenation of fluorinated N′-aryl-N- propargyl amidines for the synthesis of imidazole derivatives under mild conditions

Author keywords

aminohalogenation; cyclization; gold; homogeneous catalysis; imidazoles

Indexed keywords

AMINOHALOGENATION; CARBALDEHYDES; CASCADE CYCLIZATION; ELECTRON WITHDRAWING GROUP; HIGH YIELD; HOMOGENEOUS CATALYSIS; IMIDAZOLE DERIVATIVES; IMIDAZOLES; N-IODOSUCCINIMIDE; PROPARGYL; SELECTFLUOR; SIGNIFICANT IMPACTS;

EID: 84872451263     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201202402     Document Type: Article
Times cited : (61)

References (116)
  • 115
    • 84864627647 scopus 로고    scopus 로고
    • For a similar radical reaction of the corresponding oxazole (which was also obtained by gold catalysis) with oxygen, see:, A. S. K. Hashmi, Maria Camila Blanco Jaimes, Andreas M. Schuster, Frank Rominger, J. Org. Chem. 2012, 77, 6394-6408; for the functionalization of these positions by a direct Alder-ene reaction, see
    • (2012) J. Org. Chem. , vol.77 , pp. 6394-6408
    • Hashmi, A.S.K.1    Jaimes, M.C.B.2    Schuster, A.M.3    Rominger, F.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.