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DOI: 10.1055/s-0030-1260923
New Developments in Putting Waste to Work
J. Lu, P. H. Toy*
The University of Hong Kong, P. R. of China
Publication History
Publication Date:
19 August 2011 (online)

Significance
Lu and Toy report a tandem Wittig reductive aldol cascade, which combines five reactions in a one-pot operation. In particular, the authors achieved the formation of the stabilized Wittig reagent B from α-halo ketones 1, followed by the Wittig reaction with aldehyde 2, reduction of the resulting enone C with HSiCl3 to silyl enol ether D and the final aldol reaction with aldehydes 2 or 3 to give products 4 or 5, respectively. Yields of up to 85% demonstrate excellent efficiency over five consecutive synthetic steps. Importantly, the silane reduction (C → D) is catalyzed by triphenyl phosphine oxide, a byproduct of the initial Wittig reaction.