Observations on the mechanism of the action of carbon disulphide upon primary and secondary amines
β Scribed by H. Shipley Fry; Wilbur V. Culp
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 354 KB
- Volume
- 52
- Category
- Article
- ISSN
- 0165-0513
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π SIMILAR VOLUMES
At 170Β°C and using ionic liquids as solvent and catalyst, primary and secondary aliphatic amines could react with dimethyl carbonate to give alkyl carbamates with good yield. Due to its insolubility, the desired carbamate solid could be recovered by simple filtration from the two-layer mixture of di
## Abstract The dithiocarbamates (DTCs) disulfiram, thiram, diethyldithiocarbamate and dimethyldithiocarbamate on the equimolar base inhibited to the same extent both the lipid peroxidation (LPO) induced by ascorbic acid (nonβenzymatic) and that stimulated by an NADPHβregenerating system with CCl~4