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Volumn 76, Issue 10, 2011, Pages 4119-4124

Organocatalyzed enantioselective Michael addition of 2-hydroxy-1,4- naphthoquinone to β,γ-unsaturated α-ketophosphonatesθ

Author keywords

[No Author keywords available]

Indexed keywords

2-HYDROXY-1 ,4-NAPHTHOQUINONE; ENANTIOSELECTIVE MICHAEL ADDITION; NAPHTHOQUINONE; PARENT STRUCTURE;

EID: 79956123196     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo2002825     Document Type: Article
Times cited : (45)

References (32)
  • 2
    • 34547198987 scopus 로고    scopus 로고
    • For selected reviews on organocatalytic asymmetric conjugate additions
    • For selected reviews on organocatalytic asymmetric conjugate additions, see: Vicario, J. L.; Badia, D.; Carrillo, L. Synthesis 2007, 2065
    • (2007) Synthesis , pp. 2065
    • Vicario, J.L.1    Badia, D.2    Carrillo, L.3
  • 13
    • 79956158304 scopus 로고    scopus 로고
    • For pioneering work on the use of these Michael acceptors in asymmetric catalysis
    • For pioneering work on the use of these Michael acceptors in asymmetric catalysis, see
  • 24
    • 53549126884 scopus 로고    scopus 로고
    • For works on the use of 2-hydroxy-1,4-naphthoquinones as Michael donors
    • For works on the use of 2-hydroxy-1,4-naphthoquinones as Michael donors, see: Rueping, M.; Sugiono, E.; Merino, E. Angew. Chem., Int. Ed. 2008, 47, 3046
    • (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 3046
    • Rueping, M.1    Sugiono, E.2    Merino, E.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.