Dess–Martin oxidation
id:
dess-martin-oxidation-260-11786758
title:
Dess–Martin oxidation
text:
The Dess–Martin oxidation is an organic reaction for the oxidation of primary alcohols to aldehydes and secondary alcohols to ketones using Dess–Martin periodinane.
It is named after the American chemists Daniel Benjamin Dess and James Cullen Martin who developed the periodinane reagent in 1983. The reaction uses a hypervalent iodine reagent similar to 2-iodoxybenzoic acid to selectively and mildly oxidize alcohols to aldehydes or ketones. The reaction is commonly conducted in chlorinated solven
brand slug:
wiki
category slug:
encyclopedia
description:
original url:
https://en.wikipedia.org/wiki/Dess%E2%80%93Martin_oxidation
date created:
date modified:
2023-12-21T00:18:59Z
main entity:
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image:
{"content_url":"https://upload.wikimedia.org/wikipedia/commons/0/08/Reaction_scheme.png","width":995,"height":477}
fields total:
13
integrity:
14