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Mild water-promoted selective deacetalisatison of acyclic acetals

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GREEN CHEMISTRY
卷 12, 期 11, 页码 1919-1921

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ROYAL SOC CHEMISTRY
DOI: 10.1039/c0gc00280a

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  1. University of Johannesburg

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Various aliphatic and aromatic dimethyl and diethyl acetals and ketals were found to hydrolyse in essentially quantitative yield when heated to 80 degrees C in neat water or aqueous medium without a catalyst or any other additive, while cyclic acetals were stable under these conditions. Selective deprotection is possible when both types of acetal are present.

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