The presence of sulfur–carbon bonds is transversal to several areas of chemistry, e.g., drug discovery, materials, and chemical biology. However, a lack of efficient and sustainable procedures for the preparation of thioaminals, the N,S-analogues of O,O-acetals, contributes to this functional group often being overlooked by the scientific community. In this work is described the formation of thioaminals in water promoted by copper(II) triflate.
CITATION STYLE
Cavaca, L. A. S., Gomes, R. F. A., & Afonso, C. A. M. (2022). Preparation of Thioaminals in Water. Molecules, 27(5). https://doi.org/10.3390/molecules27051673
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