A novelmetal-free oxidative crossesterification of alcohols has been achieved usingtrichloroisocyanuric acid as an oxidant. Thealco-hols were converted in situ into theircorrespondingacyl chlorides,which were then reacted with pri-mary and secondary aliphatic,benzylic and allylicalcohols and phenols.Awide variety of esters wasobtained in satisfactory yields
Metal-free oxidative cross esterification of alcohols via acyl chloride formation
GASPA, SILVIA;PORCHEDDU, ANDREA;
2016-01-01
Abstract
A novelmetal-free oxidative crossesterification of alcohols has been achieved usingtrichloroisocyanuric acid as an oxidant. Thealco-hols were converted in situ into theircorrespondingacyl chlorides,which were then reacted with pri-mary and secondary aliphatic,benzylic and allylicalcohols and phenols.Awide variety of esters wasobtained in satisfactory yieldsFile in questo prodotto:
File | Dimensione | Formato | |
---|---|---|---|
esteri alcoli.pdf
Solo gestori archivio
Tipologia:
versione editoriale
Dimensione
409.56 kB
Formato
Adobe PDF
|
409.56 kB | Adobe PDF | Visualizza/Apri Richiedi una copia |
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.