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Volumn 4, Issue 5, 2014, Pages 1599-1606

Highly enantioselective bioinspired epoxidation of electron-deficient olefins with H2O2 on aminopyridine mn catalysts

Author keywords

asymmetric catalysis; enantioselective; epoxidation; hydrogen peroxide; intermediate; manganese; mechanism

Indexed keywords

CATALYSTS; ELECTRONS; EPOXIDATION; HYDROGEN PEROXIDE; MANGANESE; MECHANISMS; OLEFINS;

EID: 84899821969     PISSN: 21555435     EISSN: None     Source Type: Journal    
DOI: 10.1021/cs500333c     Document Type: Article
Times cited : (119)

References (99)
  • 24
    • 0002928569 scopus 로고    scopus 로고
    • Asymmetric Oxidation of Unfunctionalized Olefins and Related Reactions
    • 2 nd ed. Ojima, I. John Wiley & Sons, Inc. New York
    • Katsuki, T. Asymmetric Oxidation of Unfunctionalized Olefins and Related Reactions. In Catalytic Asymmetric Synthesis, 2 nd ed.; Ojima, I., Ed.; John Wiley & Sons, Inc.: New York, 2000; pp 287-325.
    • (2000) Catalytic Asymmetric Synthesis , pp. 287-325
    • Katsuki, T.1
  • 25
    • 84899847607 scopus 로고    scopus 로고
    • Sustainable Asymmetric Oxidations
    • 2 nd ed. Reedijk, J. Poeppelmeier, K. Elsevier: Amsterdam
    • Bryliakov, K. P. Sustainable Asymmetric Oxidations. In Comprehensive Inorganic Chemistry II, 2 nd ed.; Reedijk, J.; Poeppelmeier, K., Eds.; Elsevier: Amsterdam, 2013; Vol. 6, pp 625-664.
    • (2013) Comprehensive Inorganic Chemistry II , vol.6 , pp. 625-664
    • Bryliakov, K.P.1
  • 58
    • 0001722739 scopus 로고    scopus 로고
    • Asymmetric Epoxidation of Electron-Deficient Alkenes
    • Denmark, S. E. John Wiley & Sons, Inc. New York
    • Porter, M. J.; Skidmore, J. Asymmetric Epoxidation of Electron-Deficient Alkenes. In Organic Reactions; Denmark, S. E., Ed.; John Wiley & Sons, Inc.: New York, 2010; Vol. 74, pp 426-672.
    • (2010) Organic Reactions , vol.74 , pp. 426-672
    • Porter, M.J.1    Skidmore, J.2
  • 71
    • 84899826921 scopus 로고    scopus 로고
    • 2]} contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from the Cambridge Crystallographic Data Centre via and from the authors
    • 2]} contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from the Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif and from the authors.
  • 91
    • 84880942317 scopus 로고    scopus 로고
    • Sun with co-workers reported a very small (0.5%) incorporation
    • 2 catalyst system. See ref 63 and the following: Wang, X.; Miao, C.; Wang, S.; Xia, C.; Sun, W. ChemCatChem 2013, 5, 2489-2494
    • (2013) ChemCatChem , vol.5 , pp. 2489
    • Wang, X.1    Miao, C.2    Wang, S.3    Xia, C.4    Sun, W.5
  • 93
    • 0001322467 scopus 로고
    • references therein
    • Byrn, M.; Calvin, M. J. Am. Chem. Soc. 1966, 88, 1916-1922 and references therein
    • (1966) J. Am. Chem. Soc. , vol.88 , pp. 1916-1922
    • Byrn, M.1    Calvin, M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.