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- W2631989056 abstract "This work describes, for the first time, Michael addition reactions of tertiary fluoro-enolates in situ generated by detrifluoroacetylation with 1-(1-(phenylsulfonyl) vinylsulfonyl)benzene. Excellent enantioselectivity and chemical yields were achieved with application of catalysts (10 mol %) derived from Cu(OTf)2 and (1S,2S)-1,2-diphenylethane-1,2-diamine. These reactions show a considerable degree of structural generality and allow the preparation of new types of biologically relevant molecules that contain quaternary C-F stereogenic carbon atoms and feature five-, six-, or seven-membered rings as well as heterocyclic 3-fluoro-2,3-dihydrochromen-4-one moieties." @default.
- W2631989056 created "2017-06-30" @default.
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- W2631989056 date "2017-07-27" @default.
- W2631989056 modified "2023-10-06" @default.
- W2631989056 title "Catalytic Enantioselective Michael Addition Reactions of Tertiary Enolates Generated by Detrifluoroacetylation" @default.
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- W2631989056 doi "https://doi.org/10.1002/chem.201702091" @default.
- W2631989056 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/28639718" @default.
- W2631989056 hasPublicationYear "2017" @default.
- W2631989056 type Work @default.