New procedures based on the oxidation by bromine-catalysed hydrogen peroxide in a two-phase system provide simple and cheap transformations of alkylamines to carbonyl derivatives (aldehydes, ketones, carboxylic acid, imides, lactams) through the corresponding acetamides.
(2001). A bromine-catalysed free-radical oxidation of acetamides from primary and secondary alkylamines by H2O2 [journal article - articolo]. In CHEMICAL COMMUNICATIONS. Retrieved from https://hdl.handle.net/10446/241650
A bromine-catalysed free-radical oxidation of acetamides from primary and secondary alkylamines by H2O2
Fontana, Francesca;
2001-01-01
Abstract
New procedures based on the oxidation by bromine-catalysed hydrogen peroxide in a two-phase system provide simple and cheap transformations of alkylamines to carbonyl derivatives (aldehydes, ketones, carboxylic acid, imides, lactams) through the corresponding acetamides.File allegato/i alla scheda:
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