Abstract
An efficient one-pot synthesis of N-aryl-substituted heterocycles by a Cu-catalyzed two-fold C–N bond formation is reported. This strategy involves a Cu I -catalyzed C–N bond-forming reaction between azoles and electron-deficient bromopyridines followed by an intramolecular sp 2 C–H amination. One of the products thus formed has been successfully used as a ligand for the synthesis of a Pd complex.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
