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Volumn 126, Issue 40, 2004, Pages 12784-12785

Copper-catalyzed enantioselective conjugate addition of Grignard reagents to acyclic enones

Author keywords

[No Author keywords available]

Indexed keywords

CARBON; CHALCONE; COPPER; GRIGNARD REAGENT; REAGENT; SILICON; UNCLASSIFIED DRUG;

EID: 5644222576     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja046632t     Document Type: Article
Times cited : (122)

References (26)
  • 4
    • 0000679263 scopus 로고    scopus 로고
    • Jacobsen, E. N., Pfaltz, A., Yamamoto, H., Eds.; Springer-Verlag: New York
    • (c) Tomioka, K.; Nagaoka, Y. In Comprehensive Asymmetric Catalysis; Jacobsen, E. N., Pfaltz, A., Yamamoto, H., Eds.; Springer-Verlag: New York, 1999; Vol. 3, pp 1105-1120.
    • (1999) Comprehensive Asymmetric Catalysis , vol.3 , pp. 1105-1120
    • Tomioka, K.1    Nagaoka, Y.2
  • 17
    • 0037415851 scopus 로고    scopus 로고
    • 3 to linear aliphatic enones (ee's = 76-93%, 20 mol % catalyst), see: Frase, P. K.; Woodward, S. Chem.-Eur. J. 2003, 9, 776-783.
    • (2003) Chem.-Eur. J. , vol.9 , pp. 776-783
    • Frase, P.K.1    Woodward, S.2
  • 21
    • 85039493312 scopus 로고    scopus 로고
    • note
    • Promising results (ee < 82%) limited to benzylideneacetone were reported in refs 4b and 4d.
  • 24
    • 85039492119 scopus 로고    scopus 로고
    • note
    • 2) evaluated provided lower selectivities.
  • 25
    • 85039509871 scopus 로고    scopus 로고
    • note
    • See Supporting Information for more details.
  • 26
    • 85039504423 scopus 로고    scopus 로고
    • note
    • 2O provided 81 with 42% ee, 78:22 regio).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.