메뉴 건너뛰기




Volumn 18, Issue 46, 2012, Pages 14638-14642

NIS-catalyzed reactions: Amidation of acetophenones and oxidative amination of propiophenones

Author keywords

acetophenones; amination; dehydrogenation; N iodosuccinimide; oxidation; propiophenones

Indexed keywords

ACETOPHENONES; ACETYL DERIVATIVES; AMIDATION; HETEROCYCLIC COMPOUND; KETOAMIDES; N-IODOSUCCINIMIDE; PROPIOPHENONE; PROPIOPHENONES; SINGLE-STEP; TERT-BUTYLHYDROPEROXIDE;

EID: 84868685103     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201202703     Document Type: Article
Times cited : (150)

References (50)
  • 4
    • 84877584203 scopus 로고    scopus 로고
    • H. Knust, M. Nettekoven, E. Pinard, O. Roche, M. Rogers-Evans, WO 2009016087, 2009
    • H. Knust, M. Nettekoven, E. Pinard, O. Roche, M. Rogers-Evans, WO 2009016087, 2009
  • 5
    • 84877577186 scopus 로고    scopus 로고
    • C. A. Crowley, N. G. J. Delaet, J. Ernst, C. G. Grove, B. Hepburn, B. King, C. J. Larson, S. Miller, K. Pryor, L. J. Shuster, WO 2007146712, 2007
    • C. A. Crowley, N. G. J. Delaet, J. Ernst, C. G. Grove, B. Hepburn, B. King, C. J. Larson, S. Miller, K. Pryor, L. J. Shuster, WO 2007146712, 2007
  • 7
    • 84877581108 scopus 로고    scopus 로고
    • D. V. Patel, R. D. J. Gless, H. Webb, K. Heather, S. K. Anandan, B. R. Aavula, WO 2008073623, 2008
    • D. V. Patel, R. D. J. Gless, H. Webb, K. Heather, S. K. Anandan, B. R. Aavula, WO 2008073623, 2008.
  • 40
    • 84877580013 scopus 로고    scopus 로고
    • R. Ando, T. Sakaki, Y. Morinaka, C. Takahashi, Y. Tamao, EP 603769 A1 19940629, 1994
    • R. Ando, T. Sakaki, Y. Morinaka, C. Takahashi, Y. Tamao, EP 603769 A1 19940629, 1994
  • 43
    • 84877586126 scopus 로고    scopus 로고
    • C. C. Chiu, R. Yang, K. S. Yang, EP 2003-8171
    • C. C. Chiu, R. Yang, K. S. Yang, EP 2003-8171
  • 49
    • 84864202887 scopus 로고    scopus 로고
    • 2-promoted coupling of acetophenones with amines was published recently, see:, However, it was noticed while preparing this manuscript that in Zhang and Wang's protocol, a large excess of amines (8 equiv, see the typical procedure) was used, and no reactions for the formation of 2-aminoketones or reactions of propiophenone derivatives with secondary amines were reported.
    • 2-promoted coupling of acetophenones with amines was published recently, see:, X. Zhang, L. Wang, Green Chem. 2012, 14, 2141. However, it was noticed while preparing this manuscript that in Zhang and Wang's protocol, a large excess of amines (8 equiv, see the typical procedure) was used, and no reactions for the formation of 2-aminoketones or reactions of propiophenone derivatives with secondary amines were reported.
    • (2012) Green Chem. , vol.14 , pp. 2141
    • Zhang, X.1    Wang, L.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.