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Volumn 28, Issue 9, 2010, Pages 1731-1735

Charge-transfer effect on chiral phosphoric acid catalyzed asymmetric Baeyer-Villiger oxidation of 3-substituted cyclobutanones using 30% aqueous H2O2 as the oxidant

Author keywords

Asymmetric catalysis; Baeyer Villiger oxidation; Bronsted acid; Charge Transfer effect; Hydrogen peroxide; Organocatalysis; Phosphoric acid

Indexed keywords


EID: 78349261591     PISSN: 1001604X     EISSN: 16147065     Source Type: Journal    
DOI: 10.1002/cjoc.201090292     Document Type: Article
Times cited : (18)

References (45)
  • 2
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    • Eds: Christmann M.; Bräse, S., Wiley-VCH, Weinheim
    • For reviews, see: (a) Bolm, C. In Asymmetric Synthesis-The Essentials, Eds.: Christmann, M.; Bräse, S., Wiley-VCH, Weinheim, 2006, pp. 57-61.
    • (2006) Asymmetric Synthesis-The Essentials , pp. 57-61
    • Bolm, C.1
  • 15
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    • Synthesis
    • (c) Fatiadi, A. J. Synthesis 1986, 249.
    • (1986) , pp. 249
    • Fatiadi, A.J.1
  • 19
    • 43149113198 scopus 로고    scopus 로고
    • Donor-acceptor interactions have been used in asymmetric catalysis to assemble chiral monodentate ligands into chelates or recycling asymmetric catalysts via formation of charge transfer complexes, for examples, see
    • Donor-acceptor interactions have been used in asymmetric catalysis to assemble chiral monodentate ligands into chelates or recycling asymmetric catalysts via formation of charge transfer complexes, for examples, see: (a) Chuzel, O.; Magnier-Bouvier, C.; Schulz, E. Tetrahedron: Asymmetry 2008, 19, 1010.
    • (2008) Tetrahedron: Asymmetry , vol.19 , pp. 1010
    • Chuzel, O.1    Magnier-Bouvier, C.2    Schulz, E.3
  • 21
    • 38349189109 scopus 로고    scopus 로고
    • Chiral phosphoric acids have been established as one type of extremely versatile organocatalysts in asymmetric catalysis, for reviews, see
    • Chiral phosphoric acids have been established as one type of extremely versatile organocatalysts in asymmetric catalysis, for reviews, see: (a) Akiyama, T. Chem. Rev. 2007, 107, 5744.
    • (2007) Chem. Rev. , vol.107 , pp. 5744
    • Akiyama, T.1
  • 24
    • 77950248809 scopus 로고    scopus 로고
    • Springer-Verlag Berlin, Berlin
    • (d) Kampen, D.; Reisinger, C. M.; List, B. In Asymmetric Organocatalysis, Vol. 291, Springer-Verlag Berlin, Berlin, 2010, pp. 395-456. For selected recent examples, see
    • (2010) Asymmetric Organocatalysis , vol.291 , pp. 395-456
    • Kampen, D.1    Reisinger, C.M.2    List, B.3
  • 25
    • 78650814651 scopus 로고    scopus 로고
    • For selected recent examples, see
    • For selected recent examples, see: (e) Liao, S.; List, B. Angew. Chem., Int. Ed. 2009, 48, 628.
    • (2009) Angew. Chem., Int. Ed. , vol.48 , pp. 628
    • Liao, S.1    List, B.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.