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Volumn 50, Issue 42, 2011, Pages 9953-9956

Generation of α,β-unsaturated iminium ions by laser flash photolysis

Author keywords

electrophilicity; kinetics; linear free energy relationships; organocatalysis; reactive intermediates

Indexed keywords

ELECTROPHILICITY; IMINIUM IONS; LASER FLASH PHOTOLYSIS; LINEAR FREE ENERGY RELATIONSHIPS; ORGANOCATALYSIS; REACTIVE INTERMEDIATE;

EID: 80053899558     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201103683     Document Type: Article
Times cited : (37)

References (82)
  • 2
  • 7
    • 48849094479 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 4638-4660
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 4638-4660
  • 9
    • 53549121402 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 6138-6171
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 6138-6171
  • 14
    • 34250157969 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 1983-1987
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 1983-1987
  • 16
    • 53549103015 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 2820-2823
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 2820-2823
  • 18
    • 55249100268 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 8723-8726
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 8723-8726
  • 21
    • 70349782276 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 5034-5037.
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 5034-5037
  • 25
    • 79851489446 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2011, 50, 1613-1616.
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 1613-1616
  • 32
    • 77956552404 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2010, 49, 6520-6523
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 6520-6523
  • 35
    • 77954320410 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2010, 49, 4997-5003
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 4997-5003
  • 54
    • 77249112184 scopus 로고    scopus 로고
    • For the generation of benzhydryl cations from tri-n-butylphosphonium tetrafluoroborates see
    • J. Ammer, H. Mayr, Macromolecules 2010, 43, 1719-1723; For the generation of benzhydryl cations from tri-n-butylphosphonium tetrafluoroborates see
    • (2010) Macromolecules , vol.43 , pp. 1719-1723
    • Ammer, J.1    Mayr, H.2
  • 56
    • 78650154831 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2010, 49, 9526-9529
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 9526-9529
  • 62
    • 13244260768 scopus 로고    scopus 로고
    • for 6 k and 6 m
    • for 6 k and 6 m:, B. Kempf, H. Mayr, Chem. Eur. J. 2005, 11, 917-927
    • (2005) Chem. Eur. J. , vol.11 , pp. 917-927
    • Kempf, B.1    Mayr, H.2
  • 65
    • 34548068809 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 6176-6179.
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 6176-6179
  • 71
    • 84874810029 scopus 로고    scopus 로고
    • For a comprehensive database of nucleophilicity and electrophilicity parameters, see: http://www.cup.lmu.de/oc/mayr/DBintro.html.
  • 72
    • 70350454007 scopus 로고    scopus 로고
    • For selected examples on the use of Equation (1) in organocatalysis see: P. G. Cozzi, F. Benfatti and L. Zoli, Angew. Chem. 2009, 121, 1339-1342
    • (2009) Angew. Chem. , vol.121 , pp. 1339-1342
    • Cozzi, P.G.1    Benfatti, F.2    Zoli, L.3
  • 73
    • 60149108649 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 1313-1316
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 1313-1316
  • 79
    • 78650090073 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2010, 49, 9685-9688.
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 9685-9688
  • 80
    • 84874806324 scopus 로고    scopus 로고
    • PhD Thesis, California Institute of Technology, 2005, 41-42. We thank Professor D. W. C. MacMillan for bringing this work to our attention
    • C. H.-M. Larsen, PhD Thesis, California Institute of Technology, 2005, pp. 41-42. We thank Professor D. W. C. MacMillan for bringing this work to our attention.
    • Larsen, C.H.-M.1
  • 81
    • 79955466588 scopus 로고    scopus 로고
    • A quantitative comparison of the overall rates of imidazolidinone and diarylprolinol ether catalyzed reactions has recently been published.
    • A quantitative comparison of the overall rates of imidazolidinone and diarylprolinol ether catalyzed reactions has recently been published:, J. B. Brazier, G. P. Hopkins, M. Jirari, S. Mutter, R. Pommereuil, L. Samulis, J. A. Platts, N. C. O. Tomkinson, Tetrahedron Lett. 2011, 52, 2783-2785.
    • (2011) Tetrahedron Lett. , vol.52 , pp. 2783-2785
    • Brazier, J.B.1    Hopkins, G.P.2    Jirari, M.3    Mutter, S.4    Pommereuil, R.5    Samulis, L.6    Platts, J.A.7    Tomkinson, N.C.O.8
  • 82
    • 84986348006 scopus 로고
    • (2S,5S)-5-Benzyl-2-tert-butyl-3-methyl-imidazolidin-4-one (1 b) was first been described in.
    • (2S,5S)-5-Benzyl-2-tert-butyl-3-methyl-imidazolidin-4-one (1 b) was first been described in:, R. Naef, D. Seebach, Helv. Chim. Acta 1985, 68, 135-143.
    • (1985) Helv. Chim. Acta , vol.68 , pp. 135-143
    • Naef, R.1    Seebach, D.2


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