Abstract
For the polarographic reduction of α,β-unsaturated ketones, it was established fairly early1 that the first two-electron step corresponds to the hydrogenation of the C=C bond in contrast with the rather vague ideas proposed to explain the reduction of α,β-unsaturated aldehydes, especially cinnamaldehyde.
On leave from J. Heyrovský Institute of Polarography, Czechoslovak Academy of Sciences, Prague.
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© 1970 Plenum Publishing Company Ltd.
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Barnes, D., Zuman, P. (1970). Polarographic Reduction of Cinnamaldehyde; Comparison with 3-Phenylpropionaldehyde and Phenylpropargylaldehyde. In: Zuman, P. (eds) Topics In Organic Polarography. Springer, Boston, MA. https://doi.org/10.1007/978-1-4684-1812-5_20
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DOI: https://doi.org/10.1007/978-1-4684-1812-5_20
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