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- W2912079440 endingPage "3907" @default.
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- W2912079440 abstract "Abstract Tertiary propargylic sulfones are of significant importance in organic synthesis and medicinal chemistry, but to date no general asymmetric synthesis approach has been developed. We disclose a versatile copper‐catalyzed sulfonylation of propargylic cyclic carbonates using sodium sulfinates that allows the construction of propargylic sulfones featuring elusive quaternary stereocenters. This method provides the first successful example of such an enantioselective propargylic sulfonylation, features high asymmetric induction, wide functional group tolerance, and scalability, and enables attractive product diversification." @default.
- W2912079440 created "2019-02-21" @default.
- W2912079440 creator A5004420842 @default.
- W2912079440 creator A5021898713 @default.
- W2912079440 creator A5065337367 @default.
- W2912079440 date "2019-02-15" @default.
- W2912079440 modified "2023-10-17" @default.
- W2912079440 title "Copper‐Catalyzed Enantioselective Construction of Tertiary Propargylic Sulfones" @default.
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- W2912079440 doi "https://doi.org/10.1002/anie.201814242" @default.
- W2912079440 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30663208" @default.
- W2912079440 hasPublicationYear "2019" @default.
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