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Volumn , Issue 35, 2009, Pages 6109-6111

A general asymmetric aldol reaction of silyl ketene acetals derived from simple esters to aryl α-keto esters

Author keywords

Aldol reactions; Asymmetric catalysis; Keto esters; Synthetic methods

Indexed keywords


EID: 71549172794     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.200901086     Document Type: Article
Times cited : (13)

References (24)
  • 4
    • 71549159531 scopus 로고    scopus 로고
    • For example, methyl pyruvate gave 99 % ee, whereas ethyl pyruvate gave 91% ee
    • For example, methyl pyruvate gave 99 % ee, whereas ethyl pyruvate gave 91% ee.
  • 23
    • 34547611849 scopus 로고    scopus 로고
    • Copper Lewis Acids
    • Ed.: R. Mahrwald, Wiley-VCH, Weinheim
    • J. S. Johnson, D. A. Nicewicz, Copper Lewis Acids, in: Modern Aldol Reactions (Ed.: R. Mahrwald), Wiley-VCH, Weinheim, 2004, vol.2, pp. 69-103.
    • (2004) Modern Aldol Reactions , vol.2 , pp. 69-103
    • Johnson, J.S.1    Nicewicz, D.A.2
  • 24
    • 71549173513 scopus 로고    scopus 로고
    • The role that the aryl substituents play on the selectivity of the reaction is currently unknown
    • The role that the aryl substituents play on the selectivity of the reaction is currently unknown.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.