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Tidwell, T. T., Science of Synthesis, (2006) 23, 571.
Improved procedures for the preparation of monoalkylketenes include the pyrolysis of propanoic anhydride to form methylketene (2) (see Section 23.14.1.1.2),[37] the dehydrohalogenation of butanoyl chloride to generate ethylketene (3) for in situ stereoselective reactions (see Section 23.14.1.1.4.1),[38–46] the dehydrochlorination of propanoyl chloride for in situ stereoselective dimerization (see Section 23.14.1.2.6 ),[47] and dehalogenation of 2-bromopropanoyl bromide by zinc for conversion into the dimer (see Section 23.14.1.1.6).[48,49]
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References
[37] | Meeeee, M. M.; Meee, M.; Meeeee, M. M., M. Mee. Meee., (8888) 88, 8888. |
[38] | Meeee, M. M.; Meeee, M. M.; Meee, M.; Meeee, M.; Meeee, M. M., MMM; Meeeee, M., M. Me. Meee. Mee., (8888) 888, 8888. |
[39] | Meeeee, M.; Meee, M.; Meeee, M. M.; Meeee, M. M.; Meeeeee, M. M.; Meee, M. M.; Meeeee, M. M.; Meeeee, M., M. Me. Meee. Mee., (8888) 888, 8888. |
[40] | Meeee, M. M.; Meeee, M. M.; Meeeeee, M.; Meeeee, M., M. Me. Meee. Mee., (8888) 888, 88888. |
[41] | Meeeee, M.; Meee, M. M.; Meeeeeeeee, M.; Meee, M.; Meee, M. M.; Meeeee, M., M. Me. Meee. Mee., (8888) 888, 8888. |
[42] | Meeee, M. M.; Meeee, M. M.; Meee, M.; Meeee, M. M., MMM; Meeeee, M., Mee. Meee., (8888) 8, 8888. |
[43] | Meeeeee, M.; Meeee, M. M.; Meeee, M. M.; Meeeeee, M. M.; Meeeee, M., Mee. Meee., (8888) 8, 888. |
[44] | Meeee, M. M.; Meeee, M. M.; Meee, M.; Meeeeeeeee, M.; Meeeee, M., Mee. Meee., (8888) 8, 8888. |
[45] | Meeeee, M.; Meee, M.; Meeee, M. M.; Meeee, M. M.; Meeeee, M. M.; Meeeee, M., Mee. Meee., (8888) 8, 8888. |
[46] | Meeee, M. M.; Meeee, M. M.; Meee, M.; Meeee, M.; Meeeeeee, M.; Meeeee, M., M. Me. Meee. Mee., (8888) 888, 8888. |
[47] | Meeeee, M. M.; Mee, M. M.; Meee, M., Mee. Meee., (8888) 8, 8888. |
[48] | Meeeee, M. M., M. Mee. Meee., (8888) 88, 8888. |
[49] | Meeeee, M. M.; Mee, M., M. Mee. Meee., (8888) 88, 8888. |
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- 8.Meeeee-Meee, (8888) 8/8, 88.
- 8.Meeeee-Meee, (8888) M 88-8, 8888.