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  4. General and Practical Formation of Thiocyanates from Thiols.
 

General and Practical Formation of Thiocyanates from Thiols.

URI
https://arbor.bfh.ch/handle/arbor/32349
Version
Published
Date Issued
2014
Author(s)
Frei, Reto  
Courant, Thibaut
Wodrich, Matthew D.
Waser, Jerome
Type
Article
Language
English
Abstract
A new method for the cyanation of thiols and disulfides using cyanobenziodoxol(on)e hypervalent iodine reagents is described. Both aliphatic and aromatic thiocyanates can be accessed in good yields in a few minutes at room temperature starting from a broad range of thiols with high chemioselectivity. The complete conversion of disulfides to thiocyanates was also possible. Preliminary computational studies indicated a low energy concerted transition state for the cyanation of the thiolate anion or radical. The developed thiocyanate synthesis has broad potential for various applications in synthetic chemistry, chemical biology and materials science.
DOI
10.24451/arbor.5811
https://doi.org/10.24451/arbor.5811
Publisher DOI
10.1002/chem.201406171
Journal or Serie
Chemistry - A European Journal
ISSN
0947-6539
Organization
Architektur, Holz- und Bau  
Volume
21
Issue
6
Publisher
Wiley-Blackwell - STM
Submitter
ServiceAccount
Citation apa
Frei, R., Courant, T., Wodrich, M. D., & Waser, J. (2014). General and Practical Formation of Thiocyanates from Thiols. In Chemistry - A European Journal (Vol. 21, Issue 6, pp. 2662–2668). Wiley-Blackwell - STM. https://doi.org/10.24451/arbor.5811
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