Reactions with lead tetraacetate. I. Oxidation of saturated aliphatic alcohols. Part 1
✍ Scribed by V.M. Mićović; R.I. Mamuzić; D. Jeremić; M.Lj. Mihailović
- Publisher
- Elsevier Science
- Year
- 1963
- Tongue
- French
- Weight
- 199 KB
- Volume
- 4
- Category
- Article
- ISSN
- 0040-4039
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📜 SIMILAR VOLUMES
The lead tetraacetate (LTA) oxidation of saturated alcohols in non-polar solvents affords usually as major products unsubstituted tetrahydrofuran-type ethers, the formation of which involves intramolecular 1,5-hydrogen abstraction by the initially produced alkoxy radicals, followed by internal attac
## Abstract Oxidation of 7,8‐diaminotheophylline (1) with lead tetraacetate in refluxing toluene gave a mixture of 3‐amino‐5,7‐dimethylpyrimido[4,5‐__e__][1,2,4]triazine‐6,8‐dione (**2**) and 6‐cyanoimino‐5‐diazo‐1,3‐dimethylpyrimidine‐2,4‐dione (**4**). The latter was transformed to **2** by the r
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
## Abstract The reaction of 1, 2‐dibromo‐1, 2‐bis(4‐methoxyphenyl)ethane with alcohols was associated with rearrangement to give the corresponding bis(4‐methoxyphenyl)acetals. In boiling ethylene glycol 4,4′‐dimethoxy‐deoxybenzoin was also obtained due to an aldehyde‐ketone rearrangement. 4,4′‐Dime