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This article is cited in 6 scientific papers (total in 6 papers)
Methods of synthesis of acrolein and its α-substituted derivatives
N. A. Keiko, M. G. Voronkov Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences
Abstract:
The methods of synthesis of acrolein and its α-alkyl-substituted derivatives are examined: (a) catalytic oxidation of propene, isobutene, propane, isobutane, propyl and tert-butyl alcohols, tert-butyl alkanoates, propionaldehyde, isobutyraldehyde, and allyl alcohol and its ethers: (b) condensation of formaldehyde with aliphatic aldehydes by the Mannich reactions and also in the vapour phase over heterogeneous catalysts. Both general methods (the Mannich reaction, ipso-substitution of a α-halogen in the acrylic system, and interaction of 1-brom-2-ethoxycyclopropyllithium with electrophiles) and various special methods are used in the synthesis of the α, β-unsaturated aldehydes with functional-group-substitutents. The bibliography includes 323 references.
Received: 21.03.1993
Citation:
N. A. Keiko, M. G. Voronkov, “Methods of synthesis of acrolein and its α-substituted derivatives”, Usp. Khim., 62:8 (1993), 796–812; Russian Chem. Reviews, 62:8 (1993), 751–767
Linking options:
https://www.mathnet.ru/eng/rcr1120https://doi.org/10.1070/RC1993v062n08ABEH000045 https://www.mathnet.ru/eng/rcr/v62/i8/p796
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