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• W2033358206 abstract "Reduction of ketosulfonyl indoles with sodium borohydride provides a ready entry to tryptophols in a regiocomplementary fashion with respect to the traditional oxirane ring-opening by indoles under Friedel–Crafts conditions. Compared to traditional β-ketosulfones, ketosulfonyl indoles show a peculiar behavior since they undergo a Lewis acid promoted elimination of the arylsulfonyl group allowing the preparation of indolyl-substituted 1,4-dicarbonyl derivatives." @default.
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• W2033358206 date "2012-01-01" @default.
• W2033358206 modified "2023-10-11" @default.
• W2033358206 title "Ketosulfonyl indoles in the regiodefined synthesis of tryptophols and related indole derivatives" @default.
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• W2033358206 doi "https://doi.org/10.1039/c2ob25056j" @default.
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