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Volumn 68, Issue 37, 2012, Pages 7685-7690

Enantioselective hydrogenation of (Z)- and (E)-β-arylenamides catalyzed by rhodium complexes of monodentate chiral spiro phosphorous ligands: A new access to chiral β-arylisopropylamines

Author keywords

Arylenamides; Arylisopropylamines; Asymmetric catalysis; Chiral spiro ligands; Hydrogenation

Indexed keywords

AMIDE; LIGAND; PHOSPHINE; PHOSPHITE; PROPYLAMINE; RHODIUM COMPLEX;

EID: 84864423823     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2012.06.032     Document Type: Conference Paper
Times cited : (20)

References (42)
  • 21
    • 78650879462 scopus 로고    scopus 로고
    • The palladium-catalyzed cross coupling between enolates with amides can produce the β-arylenamides with highly Z/E selectivity; however, it is less atom-economy comparing to the above methods, see
    • Z.-H. Guang, Z.-Y. Zhang, Z.-H. Ren, Y.-Y. Wang, and X.-M. Zhang J. Org. Chem. 76 2011 339 The palladium-catalyzed cross coupling between enolates with amides can produce the β-arylenamides with highly Z/E selectivity; however, it is less atom-economy comparing to the above methods, see
    • (2011) J. Org. Chem. , vol.76 , pp. 339
    • Guang, Z.-H.1    Zhang, Z.-Y.2    Ren, Z.-H.3    Wang, Y.-Y.4    Zhang, X.-M.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.