Aromatic and aliphatic aldehydes are simply converted into esters by an efficient oxidative esterification carried out under mild conditions. The aldehydes are converted in situ into their corresponding acyl chlorides, which are then reacted with primary and secondary aliphatic, benzylic, allylic, and propargylic alcohols and phenols. A variety of esters are obtained in high yields.

Metal-free direct oxidation of aldehydes to esters using TCCA

PORCHEDDU, ANDREA;
2015-01-01

Abstract

Aromatic and aliphatic aldehydes are simply converted into esters by an efficient oxidative esterification carried out under mild conditions. The aldehydes are converted in situ into their corresponding acyl chlorides, which are then reacted with primary and secondary aliphatic, benzylic, allylic, and propargylic alcohols and phenols. A variety of esters are obtained in high yields.
2015
Organic chemistry, Physical and theoretical chemistry, Biochemistry
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11584/143941
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