Exhaustive Reduction of Esters Enabled by Nickel Catalysis.
Adam CookSekar PrakashYan-Long ZhengStephen G NewmanPublished in: Journal of the American Chemical Society (2020)
We report a one-step procedure to directly reduce unactivated aryl esters into their corresponding tolyl derivatives. This is achieved by an organosilane-mediated ester hydrosilylation reaction and subsequent Ni/NHC-catalyzed hydrogenolysis. The resulting conditions provide a direct and efficient alternative to multi-step procedures for this transformation that often require the use of hazardous metal hydrides. Applications in the synthesis of -CD3-containing products, derivatization of bioactive molecules, and chemoselective reduction in the presence of other C-O bonds are demonstrated.
Keyphrases
- ms ms
- liquid chromatography tandem mass spectrometry
- minimally invasive
- high performance liquid chromatography
- gas chromatography mass spectrometry
- simultaneous determination
- liquid chromatography
- tandem mass spectrometry
- transition metal
- mass spectrometry
- solid phase extraction
- structure activity relationship
- electron transfer