A mild and efficient method for selective cleavage of ketals and acetals using lithium chloride in water - dimethyl sulfoxide
β Scribed by Pijus Kumar Mandal; Pinak Dutta; Subhas Chandra Roy
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- French
- Weight
- 147 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
A mild and efficient neutral aqueous method for selective cleavage of acetals and ketals to the corresponding carbonyl compounds has been established by using LiCI in H20-DMSO at elevated temperature. While aryl and ~,~-unsaturated ketals and acetals underwent smooth cleavage, diaryl, non-aryl and isolated ketals and acetals remained unaffected under the reaction conditions.
π SIMILAR VOLUMES
A mild and efficient ecofriendly method for the halodecarboxylation of a,b-unsaturated aromatic acids has been developed by using lithium bromide/chloride and ceric ammonium nitrate in acetonitrile-water at room temperature to afford the vinyl halides in moderate to good yields.
Mg(HSO 4 ) 2 in the presence of wet SiO 2 was reacted with oximes, hydrazones and semicarbazones and converts them to the corresponding carbonyl compounds in good to high yields under mild and heterogeneous conditions.
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