Answers are grounded in this paper and cite their sources.
The organocatalytic enantioselective trifluoromethylthiolation of oxindoles employing N-(trifluoromethylthio)phthalimide as a stable, easy to handle CF3S-source has been developed. Optically active products with a quaternary stereogenic center bearing a CF3S-group are obtained in good yields and with good to excellent enantioselectivities.
No takes yet. Share an insight, caveat, or question.
Rueping et al. (2014) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: