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The reaction is a variation of the Hunsdiecker reaction.
An example is the Hunsdiecker reaction.
Carboxylic acids are decarboxylated in the Hunsdiecker reaction.
In the Hunsdiecker reaction, from carboxylic acids are converted to the chain-shortened halide.
The reaction mechanism of the Hunsdiecker reaction is believed to involve organic radical intermediates.
The Hunsdiecker reaction converts silver salts of carboxylic acids to alkyl halides.
Fragmentation reactions or homolysis, for instance the Norrish reaction, the Hunsdiecker reaction and certain decarboxylations.
Two methods for the synthesis of alkyl halides from carboxylic acids are the Hunsdiecker reaction and the Kochi reaction.
The Barton decarboxylation, Kolbe electrolysis, Kochi reaction and Hunsdiecker reaction are radical reactions.
A related reaction known to the West as the Hunsdiecker reaction published in 1939 by the Hunsdieckers was promoted by the Soviet Union as the Borodin reaction.
Sythesis begins with conversion of the 1,3-di-carboxylic acid of bicyclo[1.1.1]pentane 1 in a Hunsdiecker reaction to the corresponding di bromide 2 followed by a coupling reaction with n-butyllithium.
The Hunsdiecker reaction (also called the Borodin reaction after Alexander Borodin) is the organic reaction of silver salts of carboxylic acids with halogens to give organic halides.
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