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Electrochemical thiocyanation of aromatic and alkene derivatives

4th International Conference on Electrochemistry

James Y. Becker, Avishai Levy and Anna Gitkis

Ben-Gurion University of the Negev, Israel

Posters & Accepted Abstracts: Biosens J

DOI: 10.4172/2090-4967-C1-003

Abstract
The anodic thiocyanation of aromatic compounds [1, 2] showed both regio- and isomer- selectivity. For example, the parathiocyanate isomer was formed exclusively: The one-pot anodic thiocyanation and isothiocyanation of alkenes in both acidic two-phase (water-dichloromethane) and homogeneous one-phase (water-acetonitrile) media will be described too [3, 4]. A selected example of type of products obtained is illustrated in the scheme below: becker@bgu.ac.il
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