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Volumn 50, Issue 52, 2009, Pages 7297-7299

Asymmetric Michael addition of malonates to enones catalyzed by a siloxy amino acid lithium salt

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID; LITHIUM SALT; MALONIC ACID DERIVATIVE;

EID: 70449105089     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.10.033     Document Type: Article
Times cited : (32)

References (46)
  • 1
    • 52149113820 scopus 로고    scopus 로고
    • For reviews see:
    • For reviews see:. MacMillan D.W.C. Nature 455 (2009) 304
    • (2009) Nature , vol.455 , pp. 304
    • MacMillan, D.W.C.1
  • 5
    • 47749122232 scopus 로고    scopus 로고
    • Berkessel A., and Gröger H. (Eds), Wiley-VCH, Weinheim
    • In: Berkessel A., and Gröger H. (Eds). Asymmetric Organocatalysis (2005), Wiley-VCH, Weinheim
    • (2005) Asymmetric Organocatalysis
  • 6
    • 67549137639 scopus 로고    scopus 로고
    • For reviews on organocatalysis using a primary amines, see:
    • For reviews on organocatalysis using a primary amines, see:. Xu L.-W., Luo J., and Lu Y. Chem. Commun. (2009) 1807
    • (2009) Chem. Commun. , pp. 1807
    • Xu, L.-W.1    Luo, J.2    Lu, Y.3
  • 45
    • 84955394357 scopus 로고    scopus 로고
    • Yamamoto H. (Ed), Wiley-VCH, Weinheim
    • In: Yamamoto H. (Ed). Lewis Acids in Organic Synthesis (2000), Wiley-VCH, Weinheim
    • (2000) Lewis Acids in Organic Synthesis
  • 46
    • 70449098078 scopus 로고    scopus 로고
    • note
    • The imine-based catalytic asymmetric Michael addition reaction of malonates to cyclopentenone usually resulted in lower yields and selectivity than cyclohexenone or cycloheptenone. See Ref. 3b,h.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.