Les Tétrachloronitrobenzènes, les Tétrachlorodinitrobenzénes; Leur Réaction avec le Méthylate de Sodium
✍ Scribed by V. S. F. Berckmans; A. F. Holleman
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 545 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0165-0513
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
**Reaction with Tetracyanoethylene of Enamines derived from Cyclohexanone** At room temperature enamines of cyclohexanone react with tetracyanoethylene (TCNE) to give substituted tetrahydroindenes **5**. The structures are assigned on the basis of ^13^C‐NMR. data and confirmed by hydrolysis. Spectr
The redox telomerization of vinylidene chloride with carbon tetrachloride catalyzed by iron or copper salts was thoroughly studied. The DP,, of the telomers obtained vary from 1 to 100, roughly. The concentration of the reactants and the nature of the solvents exert some effect on the molecular weig
## Abstract Nitrosyl chloride is only chlorinating in darkness and above 100°. In the sun light and at room temperature it reacts as a chlorinating, nitrosating, nitrating and oxidizing agent. With trichlorethylene in fact pentachlorethane 1,1,1,2‐tetrachloro‐2‐nitrosoethane, 1,1,1,2‐tetrachloro‐2‐
**Heterocyclic dienamines III. A re‐examination of the reaction of __Fischer__'s base on tetracyanoethylene** Depending on the order of addition, __Fischer__'s base **5** (1,3,3‐trimethyl‐2‐methylidene‐indoline) reacts 1:1 with tetracyanoethylene to give either the tricyanovinylation product **6**