A visible-light-induced C3-trifluoroethylation of quinoxalin-2-(1H)-ones has been developed using an inexpensive organic dye as a photocatalyst and commercially available 1,1,1-trifluoro-2-iodoethane as a trifluoroethyl radical source. Thi...
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Enantioselective Desymmetrization of Curcumins with 3‐Olefinic Oxindoles for the Synthesis of Spirocyclohexanoneoxindoles
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Spiro-oxindoles containing three contiguous chiral centers were synthesized with excellent diastereo- and enantioselectivities via cascade double Michael reactions of curcumins with 3-alkylideneoxindole carboxylates. The selectivities are supported by transitions state energy calculations at B3LYP//6-31g(d) level of DFT.
Abstract
An enantioselective desymmetrization of curcumins with 3-olefinic oxindoles involving a cascade double-Michael addition strategy provides direct access to spirocyclohexanone-oxindoles with complete regio- and diastereoselectivities and excellent enantioselectivities, besides good to excellent yields. The products possess three contiguous chiral centers and multiple reactive functionalities. The observed selectivities were rationalized by transitions state energy calculations at B3LYP//6-31g(d) level of DFT.
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