Studies in Acyl C−H Activation via Aryl and Alkyl to Acyl “Through Space” Migration of Palladium
摘要:
Examples of the 1,4-migration of a palladium moiety in aryl- and alkylpalladium intermediates to the acyl position of an aldehyde or formamide have been observed. The resulting acylpalladium intermediate can undergo ester or carbamate formation by reaction with an alcohol; decarbonylation, followed by beta hydride elimination to an alkene; reaction with an organomercurial to form an ester; or alkene insertion. Deuterium-labeling studies have been used to confirm the palladium migration mechanism.
Et<sub>3</sub>SiH + KO<sup>t</sup>Bu provide multiple reactive intermediates that compete in the reactions and rearrangements of benzylnitriles and indolenines
作者:Andrew J. Smith、Daniela Dimitrova、Jude N. Arokianathar、Kenneth F. Clark、Darren L. Poole、Stuart G. Leach、John A. Murphy
DOI:10.1039/d0sc04244g
日期:——
unusual because it generates multiple different types of reactive intermediates simultaneously that provide access to (i) silyl radical reactions, (ii) hydrogen atom transferreactions to closed shell molecules and to radicals, (iii) electron transfer reductions and (iv) hydride ion chemistry, giving scope for unprecedented outcomes. Until now, reactions with this reagent pair have generally been explained