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Organocatalytic enantioselective conjugate addition of nitroalkanes to trifluoromethylated 3-methyleneoxindoles

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Abstract A bifunctional squaramide catalyzed asymmetric conjugate addition of nitroalkanes to trifluoromethylated 3-methyleneoxindoles was developed, and a range of trifluoromethyl containing oxindole derivatives were obtained with generally high yields and… Click to show full abstract

Abstract A bifunctional squaramide catalyzed asymmetric conjugate addition of nitroalkanes to trifluoromethylated 3-methyleneoxindoles was developed, and a range of trifluoromethyl containing oxindole derivatives were obtained with generally high yields and enantioselectivities. The nitro functionality and oxindole scaffold in the corresponding products are versatile building blocks that readily enable many further valuable transformations.

Keywords: trifluoromethylated methyleneoxindoles; addition nitroalkanes; nitroalkanes trifluoromethylated; conjugate addition

Journal Title: Tetrahedron Letters
Year Published: 2020

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