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Nucleophilic (Phenylsulfonyl/arylthio)difluoromethylation of Aldehydes with TMSCF<sub>2</sub>Br: A Three-Component Strategy

44

Citations

42

References

2019

Year

Abstract

An efficient method for nucleophilic (phenylsulfonyl/arylthio)difluoromethylation of aldehydes with TMSCF<sub>2</sub>Br was developed. The reaction proceeds through in situ generation of difluorocarbene, which is captured by PhSO<sub>2</sub>Na or ArSNa to form the corresponding PhSO<sub>2</sub>CF<sub>2</sub><sup>-</sup> or PhSCF<sub>2</sub><sup>-</sup> anions, followed by nucleophilic addition to aldehydes to give the desired difluoromethylated products.

References

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