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Volumn 135, Issue 37, 2013, Pages 13664-13667

Pd-catalyzed Semmler-Wolff reactions for the conversion of substituted cyclohexenone oximes to primary anilines

Author keywords

[No Author keywords available]

Indexed keywords

OXIDATIVE ADDITIONS; PD CATALYST; PRODUCT YIELDS; SYNTHETIC UTILITY;

EID: 84884478134     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja4073172     Document Type: Article
Times cited : (119)

References (54)
  • 20
    • 0343523011 scopus 로고
    • Traditional Semmler-Wolff reactions often lead to mixtures of mono- and diacetylated anilines, which are treated with aqueous base to afford the primary aniline. Kelly, T. R.; Chandrakumar, N. S.; Saha, J. K. J. Org. Chem. 1989, 54, 980
    • (1989) J. Org. Chem. , vol.54 , pp. 980
    • Kelly, T.R.1    Chandrakumar, N.S.2    Saha, J.K.3
  • 39
    • 0141782253 scopus 로고    scopus 로고
    • Primary anilines have been accessed via dehydrogenation of amino cyclohexene derivatives obtained via Diels-Alder cycloaddition of Cbz-protected dienamines and activated dienophiles, such as N -methyl maleimide. Neumann, H.; von Wangelin, A. J.; Klaus, S.; Strübing, D.; Gördes, D.; Beller, M. Angew. Chem., Int. Ed. 2003, 42, 4503
    • (2003) Angew. Chem., Int. Ed. , vol.42 , pp. 4503
    • Neumann, H.1    Von Wangelin, A.J.2    Klaus, S.3    Strübing, D.4    Gördes, D.5    Beller, M.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.