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.
Original language | English |
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Pages (from-to) | 3941-3944 |
Number of pages | 4 |
Journal | Journal of Organic Chemistry |
Volume | 88 |
Issue number | 6 |
DOIs | |
Publication status | Published - 17 Mar 2023 |
Austrian Fields of Science 2012
- 104015 Organic chemistry