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Recently, Odom reported the β-alkylation of the N-phenyl imine of 1-acetylcyclohexene, which was prepared in situ by Ti-mediated hydroamination of cyclohexenylacetylene: Cao, C.; Li, Y.; Shi, Y.; Odom, A. L. Chem. Commun. 2004, 2002.
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33646582685
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note
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2 at 50 °C was carried out to 75% conversion to the Z isomer exclusively, and then the temperature was increased to 150 °C. After 1 h, a 1:2 Z:E ratio was obtained, indicating that the product is susceptible to isomerization.
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23
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0001442058
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Ishikawa, M.; Matsuguchi, A.; Furumori, K.; Ohshita, J. J. Org. Chem. 1990, 55, 3277.
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33646589355
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note
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A similar electrocyclization has been reported (see ref 4).
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