메뉴 건너뛰기




Volumn , Issue 13, 2000, Pages 2055-2066

Polystyrene and polymethacrylate resin-supported Jacobsen's alkene epoxidation catalyst

Author keywords

[No Author keywords available]

Indexed keywords

ACRYLICS; CATALYST ACTIVITY; CATALYST SELECTIVITY; MOLECULAR STRUCTURE; OLEFINS; ORGANOMETALLICS; POLYSTYRENES; RESINS;

EID: 0034617308     PISSN: 14704358     EISSN: None     Source Type: Journal    
DOI: 10.1039/b002118k     Document Type: Article
Times cited : (133)

References (63)
  • 2
    • 0003703778 scopus 로고    scopus 로고
    • eds. A. W. Czarnik and S. H. De Witt, Am. Chem. Soc., Washington, USA
    • A Practical Guide to Combinatorial Chemistry, eds. A. W. Czarnik and S. H. De Witt, Am. Chem. Soc., Washington, USA, 1997.
    • (1997) A Practical Guide to Combinatorial Chemistry
  • 25
    • 0002578608 scopus 로고
    • Asymmetric Catalytic Epoxidation of Unfunctionalised Olefins
    • ed. I. Ojima, VCH, New York
    • E. N. Jacobsen, Asymmetric Catalytic Epoxidation of Unfunctionalised Olefins, in Catalytic Asymmetric Synthesis, ed. I. Ojima, VCH, New York, 1993, p. 159;
    • (1993) Catalytic Asymmetric Synthesis , pp. 159
    • Jacobsen, E.N.1
  • 26
    • 0001405437 scopus 로고
    • Transition Metal-Catalysed Oxidations: Asymmetric Epoxidations
    • eds. E. W. Abel, F. G. A. Stone and E. Wilkinson, Pergamon, New York
    • E. N. Jacobsen, Transition Metal-Catalysed Oxidations: Asymmetric Epoxidations, in Comprehensive Organometallic Chemistry, II, eds. E. W. Abel, F. G. A. Stone and E. Wilkinson, Pergamon, New York, 1995, Vol. 12, p. 1097.
    • (1995) Comprehensive Organometallic Chemistry, II , vol.12 , pp. 1097
    • Jacobsen, E.N.1
  • 49
    • 33645921239 scopus 로고    scopus 로고
    • PhD Thesis, University of Strathclyde, Glasgow, Scotland
    • L. Canali, PhD Thesis, University of Strathclyde, Glasgow, Scotland, 1998.
    • (1998)
    • Canali, L.1
  • 54
    • 33645916632 scopus 로고    scopus 로고
    • For a high quality colour photograph illustrating these colour changes see the front cover of issue No. 21, Chem. Commun., 1998.
    • (1998) Chem. Commun.
  • 56
    • 33645952594 scopus 로고    scopus 로고
    • No assignment of absolute stereochemistry was possible with this substrate due to the absence of a pure standard - hence this substrate was hot examined extensively
    • No assignment of absolute stereochemistry was possible with this substrate due to the absence of a pure standard - hence this substrate was hot examined extensively.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.