Silicon in organosulphur chemistry. Part 1. Synthesis of trisulphides
β Scribed by Giuseppe Capozzi; Antonella Capperucci; Alessandro Degl'Innocenti; Rosa Del Duce; Stefano Menichetti
- Publisher
- Elsevier Science
- Year
- 1989
- Tongue
- French
- Weight
- 200 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
The reaction of bis(trimethylsilyl)sulphide with thiosulphinates and thiosulphonates in an inert solvent under neutral and mild conditions gives symmetrical alkyl-or aryl-trisulphides.
Little attention has been devoted to the synthesis of organic trisulphides, although this class of compounds seems highly promising from the reactional point of view. They have been prepared through a number of different methods, like the direct alkylation of alkali metal polysulphides,' the treatment of the "in situ"
π SIMILAR VOLUMES
Diethyl difluoromethylphosphonylcadmium bromide reacts with ally1 and benzyl halides in THF to give the corresponding difluoromethylenephosphonate derivatives . The reaction with ally1 bromide affords a versatile synthetic intermediate which undergoes a variety of synthetic transformations and there