Russian Journal of Organic Chemistry p. 794 - 800 (2000)
Update date:2022-08-16
Topics:
Zyk
Beloglazkina
Vatsadze
Titanyuk
Dubinskaya
A new synthetic method was developed for β,β′-dihaloalkyl sulfides (halogen chlorine or bromine) by reaction of thiobisamines with olefins and alkynes in the presence of the appropriate phosphorus halides. The reaction proceeds along electrophilic mechanism affording trans-addition products. The highest yields of the target products were obtained at POBr3 or POCl3 application.
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