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Volumn 10, Issue 25, 2012, Pages 4864-4877

Catalyst development for organocatalytic hydrosilylation of aromatic ketones and ketimines

Author keywords

[No Author keywords available]

Indexed keywords

AROMATIC COMPOUNDS; CATALYSTS; ENANTIOSELECTIVITY; HYDROSILYLATION; NITROGEN COMPOUNDS; ORGANIC ACIDS;

EID: 84862207488     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/c2ob25472g     Document Type: Article
Times cited : (34)

References (95)
  • 16
    • 84891036468 scopus 로고    scopus 로고
    • Chiral Lewis bases as catalysts
    • in, ed. I. Dalko, Wiley-VCH Verlag GmbH, Weinheim, p. 255
    • P. Kočovský and A. V. Malkov, Chiral Lewis bases as catalysts, in Enantioselective Organocatalysis, ed., P. I. Dalko, Wiley-VCH Verlag GmbH, Weinheim, 2007, p. 255
    • (2007) Enantioselective Organocatalysis
    • Kočovský, P.1    Malkov, A.V.2
  • 19
    • 84872750140 scopus 로고    scopus 로고
    • Reduction of imines with trichlorosilane catalyzed by chiral Lewis bases
    • in, ed. T. Nugent, J. Wiley & Sons, Chichester, p. 131
    • P. Kočovský and S. Stončius, Reduction of imines with trichlorosilane catalyzed by chiral Lewis bases, in Chiral Amine Synthesis (Methods, Developments and Applications), ed., T. Nugent, J. Wiley & Sons, Chichester, 2010, p. 131
    • (2010) Chiral Amine Synthesis (Methods, Developments and Applications)
    • Kočovský, P.1    Stončius, S.2
  • 21
    • 84891014400 scopus 로고    scopus 로고
    • Organocatalytic enantioselective reduction of olefins, ketones, and imines
    • in, ed. I. Dalko, Wiley-VCH Verlag GmbH, Weinheim, p. 391
    • H. Kagan, Organocatalytic enantioselective reduction of olefins, ketones, and imines, in Enantioselective Organocatalysis, ed., P. I. Dalko, Wiley-VCH Verlag GmbH, Weinheim, 2007, p. 391
    • (2007) Enantioselective Organocatalysis
    • Kagan, H.1
  • 76
  • 78
    • 4644288452 scopus 로고    scopus 로고
    • The exact ee of 45 has not been established, therefore, we assumed that the mechanism of the ring opening might be a mix of SN2 and S N1
    • D. A. Klumpp R. Rendy A. McElrea Tetrahedron Lett. 2004 45 7959
    • (2004) Tetrahedron Lett. , vol.45 , pp. 7959
    • Klumpp, D.A.1    Rendy, R.2    McElrea, A.3
  • 79
    • 0039204002 scopus 로고    scopus 로고
    • Note that hydrochloric acid, which is always present in trace amounts in commercial trichlorosilane due to partial hydrolysis, appears to play a crucial role in the catalytic process since in the presence of 1,8-bis-(dimethylamino)- naphthalene and related bases the reaction completely shuts down For a recent overview of the arene-arene interaction, see
    • F. Besseau M. Luçon C. Laurence M. Berthelot J. Chem. Soc., Perkin Trans. 2 1998 101
    • (1998) J. Chem. Soc., Perkin Trans. 2 , pp. 101
    • Besseau, F.1    Luçon, M.2    Laurence, C.3    Berthelot, M.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.