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Volumn 8, Issue 24, 1997, Pages 3995-3998

Synthesis of optically active C2-symmetric ketones for the asymmetric epoxidation of prochiral olefins by dioxiranes generated in situ with Caroate(TM) as a peroxide source

Author keywords

[No Author keywords available]

Indexed keywords

EPOXIDE; KETONE;

EID: 0031584572     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(97)00559-4     Document Type: Article
Times cited : (81)

References (21)
  • 2
  • 3
    • 0002552024 scopus 로고
    • Baumstark, A. L. Ed.; JAI: Greenwich CT, Chapter I
    • (c) Curci, R. In Advances in Oxygenated Process; Baumstark, A. L. Ed.; JAI: Greenwich CT, 1990, Vol 2, Chapter I, pp. 1-59.
    • (1990) Advances in Oxygenated Process , vol.2 , pp. 1-59
    • Curci, R.1
  • 14
    • 0002578608 scopus 로고
    • Ojima, I. Ed.; VCH: New York, Chapter 4.2
    • (a) Jacobson, E. N. In Catalytic Asymmetric Synthesis; Ojima, I. Ed.; VCH: New York, 1993, Chapter 4.2, pp. 159-202.
    • (1993) Catalytic Asymmetric Synthesis , pp. 159-202
    • Jacobson, E.N.1
  • 18
    • 0344716162 scopus 로고    scopus 로고
    • note
    • With (R)-(+)-1,1′-bi-2-naphthol-derived ketone we obtained the (R,R) enantiomer of the stilbene oxide and not the reported (S,S) epoxide (Ref. 6).
  • 21
    • 0344284130 scopus 로고    scopus 로고
    • note
    • 3N solution in hexane) with hexane:ethyl acetate (1:0 to 10:1) as the eluent, to afford the epoxide 5 and the recovered ketone 3b (Table 1).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.