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- W2956804972 abstract "A highly stereoselective sequential vinylogous aldol reaction/transesterification of methyl-substituted olefinic butyrolactones and isatins was developed. With this developed protocol, a series of chiral spirocyclic oxindole-dihydropyranones were obtained in good to excellent yields (73-99%) and enantioselectivities (71-97% ee)." @default.
- W2956804972 created "2019-07-23" @default.
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- W2956804972 date "2019-01-01" @default.
- W2956804972 modified "2023-10-18" @default.
- W2956804972 title "Highly enantioselective sequential vinylogous aldol reaction/transesterification of methyl-substituted olefinic butyrolactones with isatins for the construction of chiral spirocyclic oxindole-dihydropyranones" @default.
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- W2956804972 doi "https://doi.org/10.1039/c9cc04427b" @default.
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