Preparation of Bis(dialkylcarbamoyl)mercury Compounds by Carbonylation in Amines
✍ Scribed by Prof. U. Schöllkopf; F. Gerhart
- Publisher
- John Wiley and Sons
- Year
- 1966
- Tongue
- English
- Weight
- 114 KB
- Volume
- 5
- Category
- Article
- ISSN
- 0044-8249
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✦ Synopsis
The bonds[*] between the dianion C4H629 and the
Preparation of Bis(dialkylcarbamoy1)mercury
Compounds by Carbonylation in Amines [(CH3)2AI]@ cation are very reactive; on oxidation with dry 0 2 they are preponderatingly attacked before the Al-CH3 bonds, butadiene being regenerated :
📜 SIMILAR VOLUMES
A new method for the direct conversion of oximes into aldehydes and ketones by treatment with cerium(IV) salts is described. Cerium(IV) salts can be used as an effective and mild oxidizing agent for the regeneration of carbonyl compounds from oximes in good yield. The solvent effects are discussed.
Blends of carboxyl functionalized poly(phenylene sulfide) (PPS) and poly-(ethylene terephthalate) (PET) were shown to undergo an ester interchange reaction during melt blending. Pendent carboxyl functionality randomly incorporated along the PPS chain reacts with the ester moiety of PET to form a gra