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Volumn 349, Issue 17-18, 2007, Pages 2556-2562

Rhodium-catalyzed asymmetric transfer hydrogenation of aryl alkyl ketones employing ligands derived from amino acids

Author keywords

Amino acid ligands; Asymmetric transfer hydrogenation; Ketones; Reductions; Rhodium

Indexed keywords


EID: 37349047059     PISSN: 16154150     EISSN: 15213897     Source Type: Journal    
DOI: 10.1002/adsc.200700345     Document Type: Article
Times cited : (42)

References (51)
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    • Eds, E. N. Jacobsen, A. Pfaltz, H. Yamamoto, Springer-Verlag, Berlin
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    • (1999) Comprehensive Asymmetric Catalysis , vol.1 , pp. 199
    • Ohkuma, T.1    Noyori, R.2
  • 10
    • 7044252416 scopus 로고    scopus 로고
    • Eds, E. N. Jacobsen, A. Pfaltz, H. Yamamoto, Springer Verlag, Berlin
    • T. Ohkuma, R. Noyori, Comprehensive Asymmetric Catalysis Supplement, (Eds.: E. N. Jacobsen, A. Pfaltz, H. Yamamoto), Springer Verlag, Berlin, 2004, Vol. 1, p 43.
    • (2004) Comprehensive Asymmetric Catalysis Supplement , vol.1 , pp. 43
    • Ohkuma, T.1    Noyori, R.2
  • 23
    • 33750921617 scopus 로고    scopus 로고
    • Tuning the acidities by a subtle change in the ligand structure sometimes result in a dramatic change of enantioselectivity as was observed in: A. B. Zaitsev, H. Adolfsson, Org. Lett. 2006, 8, 5129
    • Tuning the acidities by a subtle change in the ligand structure sometimes result in a dramatic change of enantioselectivity as was observed in: A. B. Zaitsev, H. Adolfsson, Org. Lett. 2006, 8, 5129.
  • 31
    • 37349121510 scopus 로고    scopus 로고
    • J. Blacker, B. Mellor, World Patent WO9842643, 1997.
    • J. Blacker, B. Mellor, World Patent WO9842643, 1997.
  • 51
    • 37349013659 scopus 로고    scopus 로고
    • The reductions of 3′-methoxyacetophenone in deuterium-labeled 2-propanol were performed as described in the general procedure presented in the Experimental Section, however, the catalyst loading was increased to 2 mol% and we used t-BuONa instead of i-PrONa as base.
    • The reductions of 3′-methoxyacetophenone in deuterium-labeled 2-propanol were performed as described in the general procedure presented in the Experimental Section, however, the catalyst loading was increased to 2 mol% and we used t-BuONa instead of i-PrONa as base.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.