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4. Oxidações QFL-5928 - Síntese Orgânica Prof. Luiz F. Silva ... - USP

4. Oxidações QFL-5928 - Síntese Orgânica Prof. Luiz F. Silva ... - USP

4. Oxidações QFL-5928 - Síntese Orgânica Prof. Luiz F. Silva ... - USP

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<strong>4.</strong> <strong>Oxidações</strong> <strong>QFL</strong>-<strong>5928</strong> - <strong>Síntese</strong> <strong>Orgânica</strong><br />

Preparação da Periodinana de Dess-Martin<br />

Preparação e Reatividade:<br />

Ireland e Liu, J. Org. Chem. 1993, 58, 2899<br />

Meyer e Schreiber, J. Org. Chem. 1994, 59, 7549.<br />

Condição típica: periodinana de Dess-Martin, CH 2Cl 2.<br />

Mecanismo simplificado:<br />

O<br />

R<br />

O<br />

2CHOH<br />

I OAc<br />

AcO OAc<br />

DMP<br />

O<br />

JACS 1978, 100, 300; JOC 1983, 48, 4155.<br />

R<br />

R<br />

O<br />

H<br />

I O<br />

AcO<br />

O<br />

O<br />

O<br />

O<br />

I<br />

OAc<br />

+<br />

R R<br />

+ AcOH<br />

The first step in DMP-oxidations is the displacement of an acetate group by<br />

the alcohol. The α-proton of the alcohol is subsequently removed by acetate<br />

(internal or external) to form the desired carbonyl compound together with an<br />

iodine(III) side product.<br />

<strong>Prof</strong>. <strong>Luiz</strong> F. <strong>Silva</strong> Jr - IQ-<strong>USP</strong> - 2012 12<br />

O

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