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• W2925154346 abstract "The diastereoselective reduction of γ-keto-sulfonates to afford α,γ-substituted γ-hydroxy sulfonates has been investigated. Herein we report the first example of a diastereoselective carbonyl reduction whereby hydride attack is directed via chelation of a neighbouring sulfonate group to a boron atom, thus affording prevalently trans γ-hydroxy sulfonates." @default.
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• W2925154346 date "2019-05-01" @default.
• W2925154346 modified "2023-10-17" @default.
• W2925154346 title "Diastereoselective sulfonate-directed carbonyl reduction of γ-keto-sulfonates" @default.
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• W2925154346 doi "https://doi.org/10.1016/j.tetlet.2019.03.065" @default.
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