Boron trifluoride promoted reaction of benzenesulphenanilides with alkenes
โ Scribed by Luisa Benati; P.Carlo Montevecchi; Piero Spagnolo
- Book ID
- 108371776
- Publisher
- Elsevier Science
- Year
- 1986
- Tongue
- French
- Weight
- 866 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0040-4020
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
N-Haloelectrophiles react with alkenes in the presence of boron trifluoride etherate to give halofluorides and N-halo adducts. There is a diverse group of positive halogen compounds containing the nitrogen-halogen bond. The group includes N-haloamines, N-haloamides, and N-haloimides. Although radic
A new efficient method for the cleavage of benzyl carbamates (CBZ protective groups) is described that involves a hard acid (BFs.OE&) -soft nucleophile (EtSH) system. Unlike other available methods, this combination avoids the reduction of olefias, acetylenes, imines, halides and nitro groups, or th