The recent surge in the applications of deuterated drug candidates has rendered an urgent need for diverse deuterium labeling techniques. Herein, an efficient Rh-catalyzed deuterated Tsuji-Wilkinson decarbonylation of naturally available aldehydes with DO is developed. In this reaction, DO not only acts as a deuterated reagent and solvent but also promotes Rh-catalyzed decarbonylation. In addition, decarbonylative strategies for the synthesis of terminal monodeuterated alkenes from α,β-unsaturated aldehydes are within reach.
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http://dx.doi.org/10.1021/jacs.2c04422 | DOI Listing |
J Am Chem Soc
June 2022
Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China.
The recent surge in the applications of deuterated drug candidates has rendered an urgent need for diverse deuterium labeling techniques. Herein, an efficient Rh-catalyzed deuterated Tsuji-Wilkinson decarbonylation of naturally available aldehydes with DO is developed. In this reaction, DO not only acts as a deuterated reagent and solvent but also promotes Rh-catalyzed decarbonylation.
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