We have devised a highly regio- and enantioselective iridium-catalyzed allylic amination reaction with the sulfur-stabilized aza-ylide, S,S-diphenylsulfilimine. This process provides a robust and scalable method for the construction of aryl-, alkyl- and alkenyl-substituted C-chiral allylic sulfilimines, which are important functional groups for organic synthesis. Additionally, the combination of the allylic amination with an in situ deprotection of the sulfilimine constitutes a convenient one-pot protocol for the construction of chiral nonracemic primary allylic amines. This journal is
CITATION STYLE
Grange, R. L., Clizbe, E. A., Counsell, E. J., & Evans, P. A. (2015). Enantioselective construction of C-chiral allylic sulfilimines via the iridium-catalyzed allylic amination with S,S-diphenylsulfilimine: Asymmetric synthesis of primary allylic amines. Chemical Science, 6(1), 777–781. https://doi.org/10.1039/c4sc01317d
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