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Volumn 3, Issue 10, 2011, Pages 1527-1529

A new motif for lewis base catalysis: Asymmetric reduction of β-enamino esters

Author keywords

amino acids; Lewis base; Organocatalysis; Reduction; Silicon

Indexed keywords


EID: 80053602163     PISSN: 18673880     EISSN: 18673899     Source Type: Journal    
DOI: 10.1002/cctc.201100210     Document Type: Article
Times cited : (23)

References (16)
  • 10
    • 70349091866 scopus 로고    scopus 로고
    • These authors note that imines and enamines are in equilibrium, and that also thwarts the preparation of the corresponding imines
    • These authors note that imines and enamines are in equilibrium, and that also thwarts the preparation of the corresponding imines: A. V. Malkov, K. Vranková, S. Stončius, P. Kočovský, J. Org. Chem. 2009, 74, 5839-5849.
    • (2009) J. Org. Chem. , vol.74 , pp. 5839-5849
    • Malkov, A.V.1    Vranková, K.2    Stončius, S.3    Kočovský, P.4
  • 11
    • 80053579013 scopus 로고    scopus 로고
    • [5] The level of enantioselectivity was low though (≤54% ee).
    • [5] The level of enantioselectivity was low though (≤54% ee).
  • 16
    • 67650573256 scopus 로고    scopus 로고
    • For a related reduction of N-acyl β-amino enones, see
    • For a related reduction of N-acyl β-amino enones, see: M. Sugiura, M. Kumahara, M. Nakajima, Chem. Commun. 2009, 3585-3587.
    • (2009) Chem. Commun. , pp. 3585-3587
    • Sugiura, M.1    Kumahara, M.2    Nakajima, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.