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Volumn 127, Issue 48, 2005, Pages 17012-17024

Enantioselective addition of secondary phosphines to methacrylonitrile: Catalysis and mechanism

Author keywords

[No Author keywords available]

Indexed keywords

AROMATIC COMPOUNDS; CATALYSIS; CATALYSTS; NICKEL; PROBABILITY DENSITY FUNCTION; PROTONS;

EID: 28844481372     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja0555163     Document Type: Article
Times cited : (149)

References (67)
  • 37
    • 28844452233 scopus 로고    scopus 로고
    • Ph.D. Thesis, No. 15593, ETH Zurich
    • (b) Fadini, L., Ph.D. Thesis, No. 15593, ETH Zurich, 2004.
    • (2004)
    • Fadini, L.1
  • 50
    • 0038626673 scopus 로고    scopus 로고
    • Gaussian, Inc.: Wallingford, CT
    • (a) Frisch, M. J.; et al. Gaussian 03; Gaussian, Inc.: Wallingford, CT, 2004.
    • (2004) Gaussian 03
    • Frisch, M.J.1
  • 57
    • 28844451637 scopus 로고    scopus 로고
    • note
    • Determination of the enantiomeric excess by chiral HPLC and GC was hampered by a slow oxidation process, and attempts to resolve stable derivatives such as phosphine sulfides and oxides by chiral HPLC and GC on OD-H and OJ cellulose columns were unsuccessful. Thus, NMR appears to be the best method for determining the % ee of the 2-cyanopropyl phosphine products.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.