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- W3036644464 endingPage "109594" @default.
- W3036644464 startingPage "109594" @default.
- W3036644464 abstract "A highly diastereoselective aldol reaction between 3-fluorooxindoles and aromatic aldehydes has been developed. Commercially available, cheap Lewis acid MgBr2OEt2 was used to promote the reaction. The reaction has a broad substrate scope with respect to both 3-fluorooxindoles and aromatic aldehydes, giving a series of α-fluoro-β-hydroxyoxindoles in good yields with high diastereoselectivities (63–94 % yield, up to 99:1 anti/syn)." @default.
- W3036644464 created "2020-06-25" @default.
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- W3036644464 date "2020-08-01" @default.
- W3036644464 modified "2023-09-27" @default.
- W3036644464 title "Highly diastereoselective aldol reactions of 3-Fluorooxindoles promoted by MgBr2•OEt2/iPr2NEt" @default.
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- W3036644464 doi "https://doi.org/10.1016/j.jfluchem.2020.109594" @default.
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