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Volumn 18, Issue 6, 2007, Pages 710-716

A structurally simple l-proline derivative promotes the asymmetric allylation of aldehydes with tribromoallyltin

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE DERIVATIVE; ALLYL COMPOUND; DICHLOROMETHANE; LEWIS BASE; PROLINE DERIVATIVE; TIN DERIVATIVE; TRIBROMOALLYLTIN; UNCLASSIFIED DRUG;

EID: 34247126420     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2007.02.025     Document Type: Article
Times cited : (19)

References (40)
  • 3
    • 34247127175 scopus 로고    scopus 로고
    • Mikami K. In Advance in Catalytic Process; Doyle, M. P., Ed.; JAI: Greenwich, 1995, p 1.
  • 5
    • 0001055858 scopus 로고    scopus 로고
    • Jacobsen E.N., Pfaltz A., and Yamamoto H. (Eds), Springer, Berlin
    • Yanagisawa A. In: Jacobsen E.N., Pfaltz A., and Yamamoto H. (Eds). Comprehensive Asymmetric Catalysis (1999), Springer, Berlin 965
    • (1999) Comprehensive Asymmetric Catalysis , pp. 965
    • Yanagisawa, A.1
  • 9
    • 0001116206 scopus 로고    scopus 로고
    • Helmchen G., Hoffmann R.W., Mulzer J., and Schaumann E. (Eds), Thieme, Stuttgart
    • Hoppe D., Roush W.R., and Thomas E.J. In: Helmchen G., Hoffmann R.W., Mulzer J., and Schaumann E. (Eds). Thomas in Stereoselective Synthesis Vol. 3 (1996), Thieme, Stuttgart 1357
    • (1996) Thomas in Stereoselective Synthesis , vol.3 , pp. 1357
    • Hoppe, D.1    Roush, W.R.2    Thomas, E.J.3
  • 33
    • 37049089583 scopus 로고
    • For an asymmetric Reformatsky reaction using indium and cinchonidine see:
    • For an asymmetric Reformatsky reaction using indium and cinchonidine see:. Johar P.S., Araki S., and Batsugan Y. J. Chem. Soc., Perkin Trans. 1 (1992) 711-713
    • (1992) J. Chem. Soc., Perkin Trans. 1 , pp. 711-713
    • Johar, P.S.1    Araki, S.2    Batsugan, Y.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.