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R. Yamaguchi, Y. Nakazono, and M. Kawanisi, Tetrahedron Lett., 24, 1801 (1983). R. Yamaguchi, Y. Nakazono, T. Matsuki, E. Hata, and M. Kawanisi. Bull. Chem. Soc. Jpn., 60, 215 (1987). R. Yamaguchi, E. Hata, T. Matsuki, and M. Kawanisi, J. Org. Chem., 52, 2094 (1987).
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46549103031
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For general reviews on N-acyliminium ions, see W. N. Speckamp and H. Hiemstra, Tetrahedron, 41, 4367 (1985). H. Hiemstra and W. N. Speckamp, in "Comprehensive Organic Synthesis," ed by B. M. Trost and I. Fleming, Pergamon Press (1991), Vol. 2, p. 1047.
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Speckamp, W.N.1
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12
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46549103031
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ed by B. M. Trost and I. Fleming, Pergamon Press
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For general reviews on N-acyliminium ions, see W. N. Speckamp and H. Hiemstra, Tetrahedron, 41, 4367 (1985). H. Hiemstra and W. N. Speckamp, in "Comprehensive Organic Synthesis," ed by B. M. Trost and I. Fleming, Pergamon Press (1991), Vol. 2, p. 1047.
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Hiemstra, H.1
Speckamp, W.N.2
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85024309081
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For reactions of N-acyliminium ions with alkynylsilanes, see T. Nishikawa, M. Isobe, and T. Goto, SYNLETT, 1991, 99.
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SYNLETT
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Nishikawa, T.1
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14
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0000964750
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2 less reactive than the latter: I. Egle, V. Gabelica, A. J. Kresge, and T. T. Tidwell, Can. J. Chem., 74, 1366 (1996).
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Organometallics
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Dallaire, C.1
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15
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0030193011
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2 less reactive than the latter: I. Egle, V. Gabelica, A. J. Kresge, and T. T. Tidwell, Can. J. Chem., 74, 1366 (1996).
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Egle, I.1
Gabelica, V.2
Kresge, A.J.3
Tidwell, T.T.4
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16
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0041652666
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note
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An use of a smaller amount (0.3 eq) of AgOTf lowered the yield to 45%.
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