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Volumn , Issue 5, 1998, Pages 543-545

Kinetic resolution of racemic allenes by using chiral (salen)manganese(III) complex as a catalyst

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EID: 0000378278     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1998-1719     Document Type: Article
Times cited : (42)

References (30)
  • 16
    • 0030968142 scopus 로고    scopus 로고
    • b) Quite recently, Mikami and co-worker reported dynamic kinetic protonation of racemic allenylmetal species, though stoichiometric amount of chiral proton source was required: Mikami, K.; Yoshida, A. Angew. Chem., Int. Ed. Engl. 1997, 36, 858-860.
    • (1997) Angew. Chem., Int. Ed. Engl. , vol.36 , pp. 858-860
    • Mikami, K.1    Yoshida, A.2
  • 25
    • 0002578608 scopus 로고
    • ed by I. Ojima, VCH publishers, Inc.: New York
    • c) Jacobsen, E. N. In "Catalytic Asymmetric Synthesis" ed by I. Ojima, VCH publishers, Inc.: New York, (1993), pp 159-202.
    • (1993) Catalytic Asymmetric Synthesis , pp. 159-202
    • Jacobsen, E.N.1
  • 26
    • 0030600176 scopus 로고    scopus 로고
    • (Salen)manganese(III) complexes have been used for the kinetic resolution of racemic conjugated olefins: a) Noguchi, Y.; Irie, R.; Fukuda, T.; Katsuki, T. Tetrahedron Lett. 1996, 37, 4533-4536.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 4533-4536
    • Noguchi, Y.1    Irie, R.2    Fukuda, T.3    Katsuki, T.4
  • 29
    • 26844453659 scopus 로고    scopus 로고
    • note
    • rel diminishes to some extent, when the substrate has an electron-withdrawing group at its phenyl group.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.