Re: ORGLIST: aldehyde oxidation

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From: JASON SMITH (jason.smith1$##$students.mq.edu.au)
Date: Thu Nov 30 2006 - 18:41:17 EST

Are we to assume that the usual suspects, Tollen's, permanganate, nitric acid, Chromium oxide and acidified dichromate do not work? Oxidation of the Wolff-Kishner product is another idea but would use similar reagents to those already mentioned. There is also the Cannizzaro reaction if you get particularly desparate.

-Jason

----- Original Message -----
From: Diogo T Carvalho <diogo$##$unilavras.edu.br>
Date: Friday, December 1, 2006 6:13 am
Subject: ORGLIST: aldehyde oxidation

> Hi!
> I need some reference or ideas on aromatic aldehyde oxidation. The
> aldehyde molecule also contains methoxy, nitro and phenolic hydroxyl
> groups. Is there any way to do it but keeping these other
> funcionalitiesintact?
> thanks
> Diogo
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