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Fluorodesulfurization of aliphatic orthothioesters

โœ 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

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โœฆ 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 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