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Volumn 37, Issue 1, 2008, Pages 2-7

Development of chiral bicyclic triazolium salt organic catalysts: The importance of the N-aryl substituent

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EID: 38949191992     PISSN: 03667022     EISSN: None     Source Type: Journal    
DOI: 10.1246/cl.2008.2     Document Type: Review
Times cited : (159)

References (57)
  • 26
    • 33748608869 scopus 로고    scopus 로고
    • Leeper has also described a chiral bicyclic triazolium salt for use in the benzoin reaction: R. L. Knight, F. J. Leeper, J. Chem. Soc., Perkin Trans. 1 1998, 1891.
    • Leeper has also described a chiral bicyclic triazolium salt for use in the benzoin reaction: R. L. Knight, F. J. Leeper, J. Chem. Soc., Perkin Trans. 1 1998, 1891.
  • 28
    • 38949118861 scopus 로고    scopus 로고
    • Chiral triazolium sait 1e is commercially available from Sigma Aldrich (Cat. No. 674788; CAS # 872143-57-2).
    • Chiral triazolium sait 1e is commercially available from Sigma Aldrich (Cat. No. 674788; CAS # 872143-57-2).
  • 35
    • 4544371662 scopus 로고    scopus 로고
    • Subsequent to our own work, several other groups have also described catalytic asymmetric Stetter reactions; see: a
    • Subsequent to our own work, several other groups have also described catalytic asymmetric Stetter reactions; see: a) J. Pesch, K. Harms, T. Bach, Eur. J. Org. Chem. 2004, 2025.
    • (2004) Eur. J. Org. Chem , pp. 2025
    • Pesch, J.1    Harms, K.2    Bach, T.3
  • 38
    • 33644652260 scopus 로고    scopus 로고
    • For a parallel study involving the asymmetric intermolecular addition of acylsilanes to enamides mediated by metallophosphite catalysts, see: M. R. Nahm, J. R. Potnick, P. S. White, J. S. Johnson, J. Am. Chem. Soc. 2006, 128, 2751
    • d) For a parallel study involving the asymmetric intermolecular addition of acylsilanes to enamides mediated by metallophosphite catalysts, see: M. R. Nahm, J. R. Potnick, P. S. White, J. S. Johnson, J. Am. Chem. Soc. 2006, 128, 2751.
  • 55
    • 33745716505 scopus 로고    scopus 로고
    • Enders et al. have published a similar study using a slightly modified triazolium salt precatalyst; see
    • Enders et al. have published a similar study using a slightly modified triazolium salt precatalyst; see: D. Enders, O. Niemeier, T. Balensiefer, Angew. Chem., Int. Ed. 2006, 45, 1463;
    • (2006) Angew. Chem., Int. Ed , vol.45 , pp. 1463
    • Enders, D.1    Niemeier, O.2    Balensiefer, T.3
  • 56
    • 0036263823 scopus 로고    scopus 로고
    • For an asymmetric intermolecular benzoin, see
    • For an asymmetric intermolecular benzoin, see: D. Enders, U. Kallfass, Angew. Chem., Int. Ed. 2002, 41, 1743.
    • (2002) Angew. Chem., Int. Ed , vol.41 , pp. 1743
    • Enders, D.1    Kallfass, U.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.