Anodic oxidation as a general route to benzoquinone bis- and mono-acetals
β Scribed by Henton, Daniel R.; Chenard, Bertrand L.; Swenton, John S.
- Book ID
- 120171590
- Publisher
- The Royal Society of Chemistry
- Year
- 1979
- Tongue
- English
- Weight
- 248 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0022-4936
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π SIMILAR VOLUMES
While the anodic oxidation of 1,4\_dimethoxybenzene itself has been extensively investigated, ' little information is available on the generality of the reaction in substituted 1,4- dialkoxybenzenes" and naphthalenes. Our need for an economical, general route to quinone bis-and monoketals prompted u
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
Synthesis of new sugar functionalized acetals has been studied using keto or ethylenic enol ethers. Complete chemoselectivity was observed for the reaction of the keto enol ether.