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• W2298506509 endingPage "8077" @default.
• W2298506509 startingPage "8069" @default.
• W2298506509 abstract "A versatile method for the rapid synthesis of diverse enantiomerically enriched lactones has been developed based on Cu-catalyzed enantioselective radical oxyfunctionalization of alkenes. The scope of this strategy encompasses a series of enantioselective difunctionalization reactions: oxyazidation, oxysulfonylation, oxyarylation, diacyloxylation, and oxyalkylation. These reactions provide straightforward access to a wide range of useful chiral lactone building blocks containing tetrasubstituted stereogenic centers, which are hard to access traditionally." @default.
• W2298506509 created "2016-06-24" @default.
• W2298506509 creator A5039233288 @default.
• W2298506509 creator A5066382350 @default.
• W2298506509 date "2015-06-23" @default.
• W2298506509 modified "2023-10-15" @default.
• W2298506509 title "Versatile Enantioselective Synthesis of Functionalized Lactones via Copper-Catalyzed Radical Oxyfunctionalization of Alkenes" @default.
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