## Abstract Double nucleophilic addition reactions of dialkoxy ketenesilyl acetals proceeded with α,β‐unsaturated imines to give 1,4‐ and 1,2‐double addition products, and their subsequent transformations afforded multisubstituted pyrroles in good yields. Application of this procedure to the synthe
Stereospecific Synthesis of β-Bromoamines by Ionic Addition of Diethyl Dibromophosphoramidate to a Double Bond
✍ Scribed by Prof. Dr. Andrzej Zwierzak; Dipl.-Chem. Krystyna Osowska
- Publisher
- John Wiley and Sons
- Year
- 1976
- Tongue
- English
- Weight
- 234 KB
- Volume
- 15
- Category
- Article
- ISSN
- 0044-8249
No coin nor oath required. For personal study only.
✦ Synopsis
It is remarkable that the deprotonation of ( ) can also follow a different route. Treatment of the solutions of ( 1 0 a ) and (lob) in ether with diisopropylethylamine gives good yields of the cyclic ketene S,N-acetals ( ) [(12a): b.p. 150°C/10-3 torr; (126): b.p. 125°C/10-3 torr].
📜 SIMILAR VOLUMES
## Intramolecular cyclization of trisilanyl ethers of homoallylalcohols proceeded regio-and stereoselectively with a 5-exo mode to give 3-(disilanylmethyl)-24latetrahydrofuran derivatives in good yields in the presence of a t-alkyl isonitrile-palladium catalyst. From the cyclized products thus obt