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CAS: 172876-97-0
MF: C10H10NOI
MW: 287.0965
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REPORT BY

Jerome Waser

Institute of Chemical Sciences and Engineering
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Co-reporter: Dr. Reto Frei;Dr. Thibaut Courant;Dr. Matthew D. Wodrich;Dr. Jerome Waser
pp: 2662-2668
Publication Date(Web):
DOI: 10.1002/chem.201406171

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.

Fu-xue Chen

Beijing Institute of Technology
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