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- W2931497469 abstract "Abstract An efficient synthesis of non-natural, diastereoselective, α-hydroxyoxoindolin appended β-aminoester derivatives has been demonstrated from unprotected Morita-Baylis-Hillman (MBH) adducts of oxindole via simple aza-Michael addition strategy. The judicious choice of sodium hydride and bulky 2,4,6-triisopropylbenzenesulphonamide provided a controlled and diastereoselective addition products with MBH adducts of oxindole for the first time." @default.
- W2931497469 created "2019-04-11" @default.
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- W2931497469 date "2020-10-01" @default.
- W2931497469 modified "2023-09-26" @default.
- W2931497469 title "Controlled and diastereoselective synthesis of α-(3-hydroxy-2 oxoindolin-3-yl)-β-aminopropanoates" @default.
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- W2931497469 doi "https://doi.org/10.1016/j.tet.2019.03.052" @default.
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