Abstract
Herein, we report a synthetic method to access a range of highly substituted indoles via the B(C6F5)3-catalyzed transfer of 2° alkyl groups from amines. The transition-metal-free catalytic approach has been demonstrated across a broad range of indoles and amine 2° alkyl donors, including various substituents on both reacting components, to access useful C(3)-alkylated indole products. The alkyl transfer process can be performed using Schlenk line techniques in combination with commercially available B(C6F5)3·nH2O and solvents, which obviates the requirement for specialized equipment (e.g., glovebox).
Cite
CITATION STYLE
Elsherbeni, S. A., Melen, R. L., Pulis, A. P., & Morrill, L. C. (2024). Accessing Highly Substituted Indoles via B(C6F5)3-Catalyzed Secondary Alkyl Group Transfer. Journal of Organic Chemistry, 89(6), 4244–4248. https://doi.org/10.1021/acs.joc.4c00025
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.