Direct Chan–Lam Amination and Etherification of Aryl BMIDA Reagents

7Citations
Citations of this article
13Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

We report a method for the direct Chan–Lam coupling of arylboronic acid N-methyliminodiacetic acid esters (ArBMIDA) with amine and alcohol nucleophiles. A wide range of C−N and C−O cross-coupled products are obtained in 34–99 % yield (34 examples). This method serves to expand the scope of organoboron components that can be used directly in this oxidative coupling reaction and provides opportunities for streamlining synthesis.

Cite

CITATION STYLE

APA

Halford-McGuff, J. M., Israel, E. M., West, M. J., Vantourout, J. C., & Watson, A. J. B. (2022). Direct Chan–Lam Amination and Etherification of Aryl BMIDA Reagents. European Journal of Organic Chemistry, 2022(45). https://doi.org/10.1002/ejoc.202200993

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free