Fluorodesulfurization of aliphatic orthothioesters
โ Scribed by Timothy B. Patrick; Christine M. Hudson
- Book ID
- 101259867
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 151 KB
- Volume
- 10
- Category
- Article
- ISSN
- 1042-7163
No coin nor oath required. For personal study only.
โฆ Synopsis
In contrast with aromatic orthothio esters that undergo desulfurative fluorination to produce trifluoromethyl substituted aromatics, aliphatic orthothio esters react with BrF with replacement of only one or two methylthio groups by fluorine. An elimination step often follows the first sulfur replacement to produce novel unsaturated fluorinated systems. แญง 1999
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## Abstract Optimized conditions are elaborated concerning the amount of Nโhalosuccinimides as oxidizing reagents.
## Abstract A number of ethyl orthothioesters has been prepared by refluxing acid chlorides with ethanethiol and zinc chloride. The substances very easily lose one mole of ethanethiol by distillation in the presence of traces of acids, affording the thioacetals of substituted ketenes VII. The struc