We have developed a highly efficient synthetic route to carbazoles that employs sequential C–C/C–N bond formation via Suzuki cross-coupling and Cadogan cyclization. The developed method is compatible with electron neutral, rich or deficient substrates. The synthetic utility of this method was demonstrated by the concise syntheses of four natural products.
Correction for ‘One-pot synthesis of carbazoles via tandem C–C cross-coupling and reductive amination’ by Deuk-Young Goo, et al., Org. Biomol. Chem., 2016, DOI: 10.1039/c5ob01952d.
Correction: One-pot synthesis of carbazoles via tandem C–C cross-coupling and reductive amination