Abstract
A practical and efficient method for the synthesis of α-fluorothioacrylamide was developed from selective defluorinative sulfuration of trifluoropropanamides with disulfides. The N-chelation-assisted copper-catalyzed defluorination and sulfurization reactions feature excellent functional group tolerance and incorporation of both sulfur atoms of disulfides into acrylamides.
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CITATION STYLE
Shen, X. Q., Wang, S. Q., Fan, D., Zhang, X. G., & Tu, H. Y. (2021). Copper-Catalyzed Selective Defluorinative Sulfuration of Trifluoropropanamides Leading to α-Fluorothioacrylamides. Journal of Organic Chemistry, 86(2), 1591–1600. https://doi.org/10.1021/acs.joc.0c02436
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