Asymmetric C–H insertion of Rh(II) stabilized carbenoids into acetals: A C–H activation protocol as a Claisen condensation equivalent

The dirhodium tetraprolinate, Rh2(S-DOSP)4 is an efficient catalyst in an enantioselective C–H activation protocol. Rh2(S-DOSP)4 catalyzed decomposition of aryldiazoacetates or vinyldiazoacetates results in the formation of transient rhodium carbenoid intermediates. These intermediates are capable of selectively inserting into the C–H bond of acetals. The resulting products are protected β-keto esters, and so the C–H activation protocol can be considered as strategically equivalent to the Claisen condensation.

Diazoacetates substituted with an electron donor group (EDG) decompose in the presence of dirhodium tetraprolinate, Rh2(S-DOSP)4, to give carbenoids which undergo regio- and stereoselective functionalizations of C–H bonds. The C–H activation of tertiary sites in acetals leads to ketals which are precursors to 1,3-keto esters, classically synthesized by a Claisen condensation.Figure optionsDownload as PowerPoint slide