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Palladium Nanoparticle-Catalyzed C−N Bond Formation. A Highly Regio- and Stereoselective Allylic Amination by Allyl Acetates

76

Citations

40

References

2009

Year

Abstract

Palladium nanoparticles, generated in situ from the reaction of palladium(II) chloride, have been demonstrated to be an efficient catalyst for C-N bond formation. A variety of aliphatic and aromatic amines have been allylated by substituted and unsubstituted allyl acetates in high yields by using palladium nanoparticles in the presence of a base without any ligand. The allylations are highly regio- and stereoselective.

References

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