Synthesis and characterization of new heterocyclic derivatives by oxidation of 1-amino-2-methylindoline
✍ Scribed by L. Peyrot; M. Elkhatib; J. R. Vignalou; R. Metz; F. Elomar; H. Delalu
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2001
- Tongue
- English
- Weight
- 191 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0022-152X
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract The synthesis of 1‐amino‐2‐methylindoline by the Raschig process was undertaken in aqueous solution. The principal side reaction that occurs in the medium is the oxidation of 1‐amino‐2‐methylindoline formed by chloramine. To increase the yield of 1‐amino‐2‐methylindoline, its oxidation
## Abstract The reaction between chloramine and 2‐methylindoline was studied at pH 12.89, __T__ = 40°C, and for different initial concentrations of reactants. The interaction includes two concurrent bimolecular mechanisms leading to 1‐amino‐2‐methylindoline and 2‐methylindole. The rate laws were de
## 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