1029654-63-4Relevant academic research and scientific papers
Preparation of phenyl-butyraldehydes using a base-catalyzed aromatization of dienones
Plano, María Fernanda,Labadie, Guillermo R.,Cravero, Raquel M.
, p. 2872 - 2874 (2008)
Seven aldehydes were prepared using a five-step sequence synthesis. The synthetic strategy involved the use of a novel aromatization reaction of dienones. These key intermediates were prepared following a sequence involving BAR of substituted tetralones,
An entry to curcuphenol/elvirol core structures via a retro-aldol reaction
Plano, Maria F.,Labadie, Guillermo R.,Jacob, Melissa R.,Tekwani, Babu L.,Cravero, Raquel M.
, p. 1098 - 1111 (2012/01/12)
Analogs of curcuphenol/elvirol, naturally occurring bisabolane sesquiterpenes, were prepared in six steps from alkyl-α-tetralones employing an aromatization reaction of cyclic dienone precursors and olefination of the key aldehyde intermediates. The in vi
