Abstract
Thirteen difluoromethyl-containing pseudopeptides were synthesized by Ugi reaction using the novel building block 2,2-difluoro-2- (phenylthio)acetic acid (2) as one component, followed by removal of the phenylsulfanyl protecting group in the presence of tributyltin hydride and azobisisobutyronitrile. © 2011 Wu et al.
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APA
Wu, J., Li, H., & Cao, S. (2011). Novel synthesis of pseudopeptides bearing a difluoromethyl group by Ugi reactionand desulfanylation. Beilstein Journal of Organic Chemistry, 7, 1070–1074. https://doi.org/10.3762/bjoc.7.123
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