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Volumn 21, Issue 12, 2015, Pages 4494-4504

Masked unsaturated esters/amides in asymmetric organocatalysis

Author keywords

Bifunctional catalysis; Enoate equivalent; Hydrogen bonds; Masked ester amide; Organocatalysis

Indexed keywords

CARBOXYLATION; CATALYSIS; ESTERIFICATION; HYDROGEN BONDS; RATE CONSTANTS; REACTION KINETICS;

EID: 84924021792     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201405552     Document Type: Article
Times cited : (38)

References (53)
  • 1
    • 0001040147 scopus 로고
    • Selected reviews on asymmetric conjugated addition
    • Selected reviews on asymmetric conjugated addition: a) B. E. Rossiter, N. M. Swingle, Chem. Rev. 1992, 92, 771-806;
    • (1992) Chem. Rev. , vol.92 , pp. 771-806
    • Rossiter, B.E.1    Swingle, N.M.2
  • 4
    • 0141725892 scopus 로고    scopus 로고
    • Selected examples: a,b-unsaturated imides
    • Selected examples: a,b-unsaturated imides: a) M. S. Taylor, E. N. Jacobsen, J. Am. Chem. Soc. 2003, 125, 11204-11205;
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 11204-11205
    • Taylor, M.S.1    Jacobsen, E.N.2
  • 7
    • 0037073238 scopus 로고    scopus 로고
    • β,γ-unsaturated α-oxophosphonates
    • d) K. Itoh, S. Kanemasa, J. Am. Chem. Soc. 2002, 124, 13394-13395; β,γ-unsaturated α-oxophosphonates:
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 13394-13395
    • Itoh, K.1    Kanemasa, S.2
  • 23
    • 0001380401 scopus 로고    scopus 로고
    • M. Sinnott Academic Press, London
    • C. W. Wharton, in Comprehensive Biological Catalysis, Vol. 1 (Ed.: M. Sinnott), Academic Press, London, 1998, pp. 345-379.
    • (1998) Comprehensive Biological Catalysis , vol.1 , pp. 345-379
    • Wharton, C.W.1
  • 52
    • 84861873661 scopus 로고    scopus 로고
    • Selected examples
    • Selected examples: a) W. Zi, W. Xie, D. Ma, J. Am. Chem. Soc. 2012, 134, 9126-9129;
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 9126-9129
    • Zi, W.1    Xie, W.2    Ma, D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.