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Pd-Catalyzed Diastereoselective Trifluoromethylthiolation of Functionalized Acrylamides

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https://figshare.com/articles/dataset/Pd-Catalyzed_Diastereoselective_Trifluoromethylthiolation_of_Functionalized_Acrylamides/5417572
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The Pd-catalyzed diastereoselective trifluoromethylthiolation of acrylamides was developed to allow the formation of the Z-isomer as a single product. Using a C–H bond functionalization strategy, the method was applied to a broad range of α-aryl, α-alkyl, and α,β-disubstituted acrylamides bearing the amide derived from the 8-aminoquinoline as a directing group. Mechanistic studies as well as postfunctionalization of the products were performed. This approach opens new routes to unprecedented SCF3-containing scaffolds.
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2017-09-18
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