Trisodium heptaphosphide in reactions with alkyl and aryl tosylates
β Scribed by V. A. Milyukov; A. V. Kataev; E. Hey-Hawkins; O. G. Sinyashin
- Book ID
- 106520392
- Publisher
- Springer
- Year
- 2007
- Tongue
- English
- Weight
- 385 KB
- Volume
- 56
- Category
- Article
- ISSN
- 1573-9171
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Reactions of trisodium heptaphosphide with half sandwich cyclopropenyl complexes of nickel gave sodium 1,2 diphosphacyclopentadienide. The influence of the ligand environment of the nickel atom on the formation of sodium 1,2 diphosphacyclopentadienide was studied.
Styrenes were alkylated with alkyl tosylates, sulfates and bromides in the presence of a zirconocene catalyst and "BuMgC1 in THF. By the use of this reaction, primary and secondary alkyl groups can be introduced regioselectively at the benzylic carbon of styrenes to give a-substituted ethylbenzenes.