Direct Synthesis of Dialkyl Ketones from Aliphatic Aldehydes through Radical <i>N</i>-Heterocyclic Carbene Catalysis
Yuki Kakeno, Mayu Kusakabe, Kazunori Nagao, Hirohisa Ohmiya
Abstract
A designed thiazolium-type N-heterocyclic carbene (NHC) catalyst having an N-neopentyl group and seven-membered backbone structure was achieved through the use of aliphatic aldehydes as acyl donors in the decarboxylative radical coupling with aliphatic carboxylic acid derived-redox active esters. The NHC catalyst also enabled the vicinal alkylacylation of vinyl arenes using aliphatic aldehydes and redox-active esters through a radical relay mechanism. These reactions provided the synthetic route to sterically hindered dialkyl ketones.
Topics & Concepts
CarbeneChemistryCatalysisSteric effectsOrganic chemistryRedoxAldehydeMedicinal chemistryN-Heterocyclic Carbenes in Organic and Inorganic ChemistryCatalytic Cross-Coupling ReactionsCatalytic C–H Functionalization Methods