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For cyclizations of dehalogenated δ-dienaminoesters, see: a
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For cyclizations of dehalogenated δ-dienaminoesters, see: (a) Cocco, M. T.; Congiu, C.; Maccioni, A.; Onnis, V. Synthesis 1992, 371.
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33845922133
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Dienaminoesters of type 6 were first reported by Bottomley who observed that an excess of methyl propiolate reacted with primary amines at 100 °C to give diadducts by a two-stage mechanism proceeding via an enaminoester (7). See: (a) Bottomley, W. Tetrahedron Lett. 1967, 21, 1997.
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Dienaminoesters of type 6 were first reported by Bottomley who observed that an excess of methyl propiolate reacted with primary amines at 100 °C to give diadducts by a two-stage mechanism proceeding via an enaminoester (7). See: (a) Bottomley, W. Tetrahedron Lett. 1967, 21, 1997.
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(b) Bottomley, W.; Phillips, J. N.; Wilson, J. G. Tetrahedron Lett. 1967, 31, 2957.
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0001326937
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For examples of tertiary dienaminoesters reacting in this fashion, see: Anghelide, N, Draghici, C, Raileanu, D. Tetrahedron 1974, 30, 623
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For examples of tertiary dienaminoesters reacting in this fashion, see: Anghelide, N.; Draghici, C.; Raileanu, D. Tetrahedron 1974, 30, 623.
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29
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(a) Agami, C.; Dechoux, L.; Hamon, L.; Severine, H. Synthesis 2003, 6, 859.
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(b) Agami, C.; Dechoux, L.; Hebbe, S. Synlett 2001, 9, 1440.
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Agami, C.1
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