Abstract
A concise and regioselective preparation of 2-heteroarylmethylene decorated N-arylpyrroles is described through a metal-free Mannich/Wittig/hydroamination sequence followed by isomerization of the N-arylpyrrolidine adducts. Furthermore, the C-H regioselective oxidation of these substrates is demonstrated, extending the molecular diversity and versatility of these scaffolds. © 2013 Jean et al.
Author supplied keywords
Cite
CITATION STYLE
Jean, A., Blanchet, J., Rouden, J., Maddaluno, J., & De Paolis, M. (2013). An organocatalytic route to 2-heteroarylmethylene decorated N-arylpyrroles. Beilstein Journal of Organic Chemistry, 9, 1480–1486. https://doi.org/10.3762/bjoc.9.168
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.