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Schmidt Rearrangment Reaction with Mechanism

Schmidt Rearrangment Reaction with MechanismУ вашего броузера проблема в совместимости с HTML5
The carboxylic acid Schmidt reaction starts with acylium ion 1 obtained from protonation and loss of water. Reaction with hydrazoic acid forms the protonated azido ketone 2, which goes through a rearrangement reaction with the alkyl group R, migrating over the C-N bond with expulsion of nitrogen.
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