Azidophosphanes: Attractive starting materials for the preparation of phosphazenes
β Scribed by Lothar Riesel; Robert Friebe; Anke Bergemann; Detlef/Sturm
- Book ID
- 102235287
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 307 KB
- Volume
- 2
- Category
- Article
- ISSN
- 1042-7163
No coin nor oath required. For personal study only.
β¦ Synopsis
Azidophosphanes are versatile reactants in the Staudinger reaction. The azides Cl2PN3 (I), (Et2N)ClPN3 (2), and (Et2N)2PN3 (3) react with phosphanes to give the N-phosphanyl phosphazenes 4-10. (Et2N)P(N3), is oxidized by PhN, yielding (Et2N)P(N3),=NPh (1 I), which with PPh3 yields the di-and triphosphazenes 12 and 13.
π SIMILAR VOLUMES
Imidoyl Chlorides as Starting Materials for the Preparation of Masked Acyllithium Intermediates: Synthetic Applications. -A new and simple synthesis of imidoyl-Li intermediates is presented, which on reaction with electrophiles afford imino and amino alcohols. These products are suitable precursors