Conversion of Alcohols to Phosphorothiolates Using a Thioiminium Salt as Coupling Agent

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Abstract

We report a method for the direct and rapid conversion of primary and secondary alcohols to the corresponding phosphorothiolates in yields ranging from 64% to 97%, using as a coupling agent the iminium salt prepared from N,N-dimethylthioformamide and Meerwein's salt. Selective reaction of primary alcohols in the presence of secondary alcohols is possible. The reaction of secondary alcohols proceeds stereospecifically with inversion of configuration.

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Grounds, H., Ermanis, K., Newgas, S. A., & Porter, M. J. (2017). Conversion of Alcohols to Phosphorothiolates Using a Thioiminium Salt as Coupling Agent. Journal of Organic Chemistry, 82(23), 12735–12739. https://doi.org/10.1021/acs.joc.7b01657

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