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- W2085192559 abstract "Dimethyl pyridine-2,6-dicarboxylate was selectively substituted through free-radical reactions. The substitution involves the generation of free radicals through Fenton-type reactions, followed by hydrogen abstraction from aldehydes or alcohols. The resultant carbon-centered acyl, alkyl, or hydroxyalkyl free radicals regioselectively attack protonated dimethyl pyridine-2,6-dicarboxylate at position 4, yielding the corresponding dimethyl 4-acyl-, 4-alkyl-, and 4-(hydroxyalkyl)pyridine-2,6-dicarboxylates. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005)" @default.
- W2085192559 created "2016-06-24" @default.
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- W2085192559 date "2005-04-01" @default.
- W2085192559 modified "2023-09-24" @default.
- W2085192559 title "Free-Radical Approach to 4-Substituted Dipicolinates" @default.
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- W2085192559 doi "https://doi.org/10.1002/ejoc.200400637" @default.
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