Answers are grounded in this paper and cite their sources.
The potential of deuterated pharmaceuticals is being widely demonstrated. Here we describe the first trideuteromethylation under radical reaction conditions using deuterated dimethyl sulfoxide as a reagent for the synthesis of labelled heterocycles and trideuteromethylated compounds. A broad scope of the developed method for the synthesis of various scaffolds was demonstrated.
No takes yet. Share an insight, caveat, or question.
Caporaso et al. (2016) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: