One-step conversion of oximes to gem-chloro-nitro derivatives
โ Scribed by Paolo Ceccherelli; Massimo Curini; Francesco Epifano; Maria Carla Marcotullio; Ornelio Rosati
- Book ID
- 108386786
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 121 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
Halo-Nitro Derivatives. -Use of wet basic alumina as support for Oxone (KHSO 5 ) and KBr is crucial for the conversion of oximes (I), (III), (V), and (VII) directly into the corresponding gem-bromo-nitro compounds. -
One-Step Conversion of C-Glycopyranosylnitromethanes to the Corresponding Methanal Oximes. -Hydride reduction of per-O-acetylated C-glycopyranosylnitromethanes (I) under radical conditions results in high yield formation of the corresponding oximes (II). -(PHAM-HUU, DUY-PHONG;