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J Org Chem ; 86(2): 1591-1600, 2021 01 15.
Artigo em Inglês | MEDLINE | ID: mdl-33372521

RESUMO

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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