On the mechanism of osazone formation
โ Scribed by Alfred Hassner; P. Catsoulacos
- Publisher
- Elsevier Science
- Year
- 1967
- Tongue
- French
- Weight
- 241 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
โฆ Synopsis
The details of the formation of bisphenylhydrazones (osazones) from ketols or aldols have long intrigued the organic chemist. A direct oxidation mechanism first suggested by Fischer' has not received much support. After Weygand proposed routes A and B for osazone formationj, evidence in favor of either pathway was presented by different investigators. 4
๐ SIMILAR VOLUMES
It is known'" that sugar phenylosazones undergo cyclization in aqueous CuSO, to give phenylosotriazoles in yields ranging from 45-70%. In order to identify the side reactions responsible for the low yields, Cu(I1) salts were treated with two bis(phenylhydrazones) and two mono(phenylhydrazones) and t
The reaction of squaric acid (1) with phenylhydrazlne yields cyclobutanetetraone poly(phenylhydrazones) (2-41, as reported earlier, as well as squaric acid derivatives, reported here. The latter products are a salt, 1,3-dianilinocyclobutenediylium-2,4\_diolate (51, and 1-anilino-2-phenylhydrazinocyc