1.
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.