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Volumn , Issue 9, 1999, Pages 855-856

New efficient method for the stereoselective synthesis of α-(trifluoromethyl)-α, β-unsaturated amides. Lewis acid-catalyzed reaction of 3,3,3-trifluoro-1-propynylamine with carbonyl compounds

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EID: 0033474081     PISSN: 03667022     EISSN: None     Source Type: Journal    
DOI: 10.1246/cl.1999.855     Document Type: Article
Times cited : (9)

References (23)
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    • Posner, G.H.1
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    • For selected reviews on the conjugate addition reactions, see: G.H. Posner, Org. React., 19, 1 (1972). B.H. Lipshutz and S. Sengupta, Org. React., 41, 135 (1992). S.G. Davies and O. Ichihara, J. Synth. Org. Chem. Jpn., 55, 26 (1997).
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  • 3
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    • For selected reviews on the conjugate addition reactions, see: G.H. Posner, Org. React., 19, 1 (1972). B.H. Lipshutz and S. Sengupta, Org. React., 41, 135 (1992). S.G. Davies and O. Ichihara, J. Synth. Org. Chem. Jpn., 55, 26 (1997).
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    • 0003523008 scopus 로고
    • Pergamon Press, Oxford
    • W. Carruthers, "Cycloaddition Reactions in Organic Synthesis," Pergamon Press, Oxford (1990). For reviews on the Diels-Alder reactions, see: H. L. Holmes, Org. React., 4, 60 (1948). E. Ciganek, Org. React., 32, 1 (1984).
    • (1990) Cycloaddition Reactions in Organic Synthesis
    • Carruthers, W.1
  • 5
    • 0001907371 scopus 로고
    • W. Carruthers, "Cycloaddition Reactions in Organic Synthesis," Pergamon Press, Oxford (1990). For reviews on the Diels-Alder reactions, see: H. L. Holmes, Org. React., 4, 60 (1948). E. Ciganek, Org. React., 32, 1 (1984).
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    • Holmes, H.L.1
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    • 0003009874 scopus 로고
    • W. Carruthers, "Cycloaddition Reactions in Organic Synthesis," Pergamon Press, Oxford (1990). For reviews on the Diels-Alder reactions, see: H. L. Holmes, Org. React., 4, 60 (1948). E. Ciganek, Org. React., 32, 1 (1984).
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    • Ciganek, E.1
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    • 0004101860 scopus 로고
    • John Wiley & Sons, New York
    • A. Padwa, "1,3-Dipolar Cycloaddition Chemistry," John Wiley & Sons, New York (1984), Vols. 1 and 2 . For a review on the 1,3-dipolar cycloaddition reactions, see: P.N. Confalone and E.M. Huie, Org. React., 36, 1 (1988).
    • (1984) 1,3-Dipolar Cycloaddition Chemistry , vol.1-2
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    • 0002294391 scopus 로고
    • A. Padwa, "1,3-Dipolar Cycloaddition Chemistry," John Wiley & Sons, New York (1984), Vols. 1 and 2 . For a review on the 1,3-dipolar cycloaddition reactions, see: P.N. Confalone and E.M. Huie, Org. React., 36, 1 (1988).
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    • Confalone, P.N.1    Huie, E.M.2
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    • It was reported that nonfluorinated alkynylamine reacted with carbonyl compounds even in the presence or absence of Lewis acid R. Fuks, R. Buijle, and H.G. Viehe, Angew. Chem., Int. Ed. Engl., 5, 585 (1966). R. Fuks and H.G. Viehe, Chem. Ber., 103, 564 (1970).
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    • Fuks, R.1    Buijle, R.2    Viehe, H.G.3
  • 16
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    • It was reported that nonfluorinated alkynylamine reacted with carbonyl compounds even in the presence or absence of Lewis acid R. Fuks, R. Buijle, and H.G. Viehe, Angew. Chem., Int. Ed. Engl., 5, 585 (1966). R. Fuks and H.G. Viehe, Chem. Ber., 103, 564 (1970).
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    • note
    • 19F (84 MHz) NMR) and analytical data.
  • 19
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    • note
    • 14
  • 20


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