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3-Bromopropenyl acetate was obtained as a 75:25 mixture of E/Z isomers and 3-bromopropenyl benzoate was obtained following two different experimental procedures as a 45:55 mixture of E/Z isomers and as the pure E isomer. For more details of the experimental procedures, see: M. Lombardo, S. Morganti, C. Trombini, J. Org. Chem. 2003, 68, 997.
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3-Bromopropenyl acetate was obtained as a 75:25 mixture of E/Z isomers and 3-bromopropenyl benzoate was obtained following two different experimental procedures as a 45:55 mixture of E/Z isomers and as the pure E isomer. For more details of the experimental procedures, see: M. Lombardo, S. Morganti, C. Trombini, J. Org. Chem. 2003, 68, 997.
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It has been reported that the main drawback associated with this process is the occurrence of intra- and intermolecular acyl transfer reactions associated with the nucleophilicity of the organoindium intermediates.[15
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It has been reported that the main drawback associated with this process is the occurrence of intra- and intermolecular acyl transfer reactions associated with the nucleophilicity of the organoindium intermediates.[15]
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Lombardo et al. has studied the chromium-catalyzed reaction of cyclohexanecarbaldehyde with 3-bromopropenyl acetate, which affords mixtures of type I and II compounds, see: M. Lombardo, S. Morganti, S. Licciulli, C. Trombini, Synlett 2003, 43.
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Lombardo et al. has studied the chromium-catalyzed reaction of cyclohexanecarbaldehyde with 3-bromopropenyl acetate, which affords mixtures of type I and II compounds, see: M. Lombardo, S. Morganti, S. Licciulli, C. Trombini, Synlett 2003, 43.
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