Wotal, A., and D. Weix. Synthesis of Functionalized Dialkyl Ketones from Carboxylic Acid Derivatives and Alkyl Halides. Org. Lett., 1479.
| Abstract | Unsymmetrical dialkyl ketones can be directly prepared by the nickel-catalyzed reductive coupling of carboxylic acid chlorides or (2-pyridyl)thioesters with alkyl iodides or benzylic chlorides. A wide variety of functional groups are tolerated by this process, including common nitrogen protecting groups and C–B bonds. Even hindered ketones flanked by tertiary and secondary centers can be formed. The mechanism is proposed to involve the reaction of a (L)Ni(alkyl)2 intermediate with the carboxylic acid derivative. |
| Keywords | acyl chlorides, anhydrides, aryl halides, carbon bond formation, complexes, convenient, cross-coupling reactions, organozinc reagents, palladium, thiol esters |
| DOI | 10.1021/ol300217x |