Abstract
AbstractA new diversified, rapid and easily accessible, N‐heterocyclic carbene based palladacycle, SingaCycleTM‐A1 exploited for the cross coupling reactions on heterocyclic amines. This Pd‐NHC catalyst is considered to be merely stable and takes part in dynamic conversion of various organic functionalities. Herein, we report its first time use in the synthesis of C‐ and N‐ diaryl/ heteroaryl pyridine analogues from the less active parent 5‐bromopyridine‐2‐amine via sequential Suzuki‐Miyaura and Buchwald couplings. Surprisingly, both the coupling reactions proceed very smoothly and efficiently under mild reaction conditions in green solvent system (ethanol:water) at a faster rate. Moreover 1 mol% of the catalyst is sufficient to proceed the reactions and obtain comparatively better results.
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.
