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Volumn 3, Issue 3, 2012, Pages 842-845

Highly stereoselective catalytic conjugate addition of acyl anion equivalent to nitroolefins

Author keywords

[No Author keywords available]

Indexed keywords

ACYL ANIONS; AZLACTONES; CONJUGATE ADDITION; ENANTIOSELECTIVE CONJUGATE ADDITION; MOLECULAR ASSOCIATIONS; NITROOLEFINS; OPTICALLY ACTIVE; POLARITY DEPENDENCE; PROTON DONORS; STEREO-SELECTIVE;

EID: 84857344995     PISSN: 20416520     EISSN: 20416539     Source Type: Journal    
DOI: 10.1039/c1sc00678a     Document Type: Article
Times cited : (54)

References (15)
  • 5
    • 77949418594 scopus 로고    scopus 로고
    • For reviews on organocatalytic asymmetric conjugate additions, see
    • D. Rix J. Lacour Angew. Chem., Int. Ed. 2010 49 1918
    • (2010) Angew. Chem., Int. Ed. , vol.49 , pp. 1918
    • Rix, D.1    Lacour, J.2
  • 9
    • 0036089366 scopus 로고    scopus 로고
    • Only two examples of the stereoselective conjugate addition of 2,4-disubstituted azlactones to nitroalkenes at 2-position were reported. See
    • O. M. Berner L. Tedeschi D. Enders Eur. J. Org. Chem. 2002 1877
    • (2002) Eur. J. Org. Chem. , pp. 1877
    • Berner, O.M.1    Tedeschi, L.2    Enders, D.3
  • 12
    • 0142004024 scopus 로고    scopus 로고
    • a (9.82 for PhOH, see ref. 8) and the structure of the phenolic components
    • G. Schüürmann J. Chem. Phys. 1998 109 9523
    • (1998) J. Chem. Phys. , vol.109 , pp. 9523
    • Schüürmann, G.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.