Babler oxidation

id: babler-oxidation-281-7531598
title: Babler oxidation
text: The Babler oxidation, also known as the Babler-Dauben oxidation, is an organic reaction for the oxidative transposition of tertiary allylic alcohols to enones using pyridinium chlorochromate (PCC): It is named after James Babler who first reported the reaction in 1976 and William Dauben who extended the scope to cyclic systems in 1977, thereby significantly increasing the synthetic utility: The reaction produces the desired enone product to high yield (typically >75%), is operationally simple an
brand slug: wiki
category slug: encyclopedia
description:
original url: https://en.wikipedia.org/wiki/Babler_oxidation
date created:
date modified: 2022-05-19T11:07:58Z
main entity: {"identifier":"Q2139237","url":"https://www.wikidata.org/entity/Q2139237"}
image: {"content_url":"https://upload.wikimedia.org/wikipedia/commons/1/11/Dauben_oxidation_en.svg","width":444,"height":158}
fields total: 13
integrity: 14

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