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Volumn 125, Issue 4, 2004, Pages 603-607

Synthesis of highly 1,3-proton shift transferable N-benzyl imines reaction conditions

Author keywords

1,3 Proton shift reaction; Fluorine and compounds; Imines; Operationally convenient conditions

Indexed keywords

ACETIC ACID; ACETOPHENONE DERIVATIVE; BENZYLAMINE; CARBONYL DERIVATIVE; FLUORINE DERIVATIVE; IMINE; PROTON;

EID: 2342514097     PISSN: 00221139     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jfluchem.2003.11.032     Document Type: Article
Times cited : (34)

References (67)
  • 1
    • 0003490830 scopus 로고
    • For recent, excellently edited and comprehensive monographs on synthesis and application of fluoro-organic compounds in general and fluorine-containing amino-compounds in particular, see (Eds.) Elsevier, Amsterdam, The Netherlands
    • For recent, excellently edited and comprehensive monographs on synthesis and application of fluoro-organic compounds in general and fluorine-containing amino-compounds in particular, see: R. Filler, Y. Kobayashi, L.M. Yagupolskii (Eds.), Organofluorine in Medicinal Chemistry and Biochemical Applications, Elsevier, Amsterdam, The Netherlands, 1993
    • (1993) Organofluorine in Medicinal Chemistry and Biochemical Applications
    • Filler, R.1    Kobayashi, Y.2    Yagupolskii, L.M.3
  • 6
    • 43949152987 scopus 로고
    • For comprehensive reviews on fluorine-containing amino acids and asymmetric synthesis of fluorinated compounds, see (Eds.) Wiley, Chichester, UK
    • For comprehensive reviews on fluorine-containing amino acids and asymmetric synthesis of fluorinated compounds, see: V.P. Kukhar, V.A. Soloshonok, (Eds.) Fluorine-Containing Amino Acids, Wiley, Chichester, UK, 1994
    • (1994) Fluorine-Containing Amino Acids
    • Kukhar, V.P.1    Soloshonok, V.A.2
  • 10
    • 0042074655 scopus 로고    scopus 로고
    • For recent leading publications on synthesis and application of α-trifluoromethyl containing amines, see
    • For recent leading publications on synthesis and application of α-trifluoromethyl containing amines, see: Legros J.Meyer F.Coliboeuf M.Crousse B.Bonnet-Delpon D.Begue J.-P. J. Org. Chem. 68 2003 6444
    • (2003) J. Org. Chem. , vol.68 , pp. 6444
    • Legros, J.1    Meyer, F.2    Coliboeuf, M.3    Crousse, B.4    Bonnet-Delpon, D.5    Begue, J.-P.6
  • 21
    • 0032513257 scopus 로고    scopus 로고
    • For reviews on the use of (R)- and (S)-α-phenylethylamine in asymmetric synthesis, see
    • For reviews on the use of (R)- and (S)-α-phenylethylamine in asymmetric synthesis, see: Juaristi E.Escalante J.León-Romo J.L.Reyes A. Tetrahedron: Asymmetry 9 1998 715
    • (1998) Tetrahedron: Asymmetry , vol.9 , pp. 715
    • Juaristi, E.1    Escalante, J.2    León-Romo, J.L.3    Reyes, A.4
  • 23
    • 0030590464 scopus 로고    scopus 로고
    • Steric bulk and stereocontrolling properties of trifluoromethyl group, as well as fluorine-containing substituents, are still controversial issues. For some discussions, see
    • Steric bulk and stereocontrolling properties of trifluoromethyl group, as well as fluorine-containing substituents, are still controversial issues. For some discussions, see: Soloshonok V.A. Avilov D.V. Kukhar V.P. Tetrahedron 52 1996 12433
    • (1996) Tetrahedron , vol.52 , pp. 12433
    • Soloshonok, V.A.1    Avilov, D.V.2    Kukhar, V.P.3
  • 41
    • 0003490503 scopus 로고
    • P.M. Fasella, A.E. Braunstein, A. Rossi-Fanelli, (Eds.) Macmillan, New York
    • Snell E.E. in: P.M. Fasella, A.E. Braunstein, A. Rossi-Fanelli, (Eds.), Chemical and Biological Aspects of Pyridoxal Catalysis, Macmillan, New York, 1963, pp. 1-12
    • (1963) Chemical and Biological Aspects of Pyridoxal Catalysis , pp. 1-12
    • Snell, E.E.1
  • 44
    • 84912286636 scopus 로고
    • M. Florkin, E.H. Stotz, (Eds.) Elsevier, New York Chapter 5
    • Guirard B.M. Snell E.E. in: M. Florkin, E.H. Stotz, (Eds.) Comprehensive Biochemistry, vol. 15, Elsevier, New York, 1964, Chapter 5
    • (1964) Comprehensive Biochemistry , vol.15
    • Guirard, B.M.1    Snell, E.E.2
  • 51
    • 0027156061 scopus 로고
    • For preparation of fluorine-containing α- and β-amino acids using PSR methodology see
    • For preparation of fluorine-containing α- and β-amino acids using PSR methodology see: Soloshonok V.A. Kirilenko A.G. Kukhar V.P. Resnati G. Tetrahedron Lett. 34 1993 3621
    • (1993) Tetrahedron Lett. , vol.34 , pp. 3621
    • Soloshonok, V.A.1    Kirilenko, A.G.2    Kukhar, V.P.3    Resnati, G.4
  • 60
    • 0013315761 scopus 로고
    • For application of PSR methodology for preparing fluorine-free amino-compounds see
    • For application of PSR methodology for preparing fluorine-free amino-compounds see: Johannes W.G.H. Johannes V.G. Roeland N.J.M. Binne Z. Tetrahedron Lett. 36 1995 3917
    • (1995) Tetrahedron Lett. , vol.36 , pp. 3917
    • Johannes, W.G.H.1    Johannes, V.G.2    Roeland, N.J.M.3    Binne, Z.4
  • 63
    • 0013227127 scopus 로고    scopus 로고
    • For application of PSR methodology for preparing fluorinated P-amino acids see
    • For application of PSR methodology for preparing fluorinated P-amino acids see: Chengye Y. Youji Huaxue 21 2001 862
    • (2001) Youji Huaxue , vol.21 , pp. 862
    • Chengye, Y.1
  • 66
    • 0037416951 scopus 로고    scopus 로고
    • For application of PSR methodology for preparing fluorinated P-amino acids see
    • For application of PSR methodology for preparing fluorinated P-amino acids see: Ohkura H. Berbasov D.O. Soloshonok V.A. Tetrahedron 59 2003 1647
    • (2003) Tetrahedron , vol.59 , pp. 1647
    • Ohkura, H.1    Berbasov, D.O.2    Soloshonok, V.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.