Abstract
We report the development of an isothiouronium salt as a reagent for the operationally simple synthesis of cyanomethyl thioesters with high functional group tolerance and avoiding the use of thiols. Additionally, we show that the products can be engaged in amide synthesis in either a two-step or one-pot fashion.
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CITATION STYLE
APA
Tiefenbrunner, I., Brutiu, B. R., Stopka, T., & Maulide, N. (2023). Isothiouronium-Mediated Conversion of Carboxylic Acids to Cyanomethyl Thioesters. Journal of Organic Chemistry, 88(6), 3941–3944. https://doi.org/10.1021/acs.joc.2c02902
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