A number of dibenzylidenecycloalkanones were prepared by a base condensation reaction of the cycloalkanone with benzaldehyde or a substituted benzaldehyde. The products were then subjected to a mixed hydride reagent (3 AlCl3-1 LiAlH4) to give olefins or tautomeric mixtures depending on the method of reaction.
Proceedings of the Iowa Academy of Science
© Copyright 1972 by the Iowa Academy of Science, Inc.
Privett, James E.; Miller, Rodger; and Stidfole, Leon
"Preparation of Dibenzylidenecycloalkanones and Their Mixed Hydride Reductions,"
Proceedings of the Iowa Academy of Science, 79(2), 53-55.
Available at: https://scholarworks.uni.edu/pias/vol79/iss2/4