Abstract

AbstractWhereas aryl(trialkyl)silanes are considered to be ideal organometallic reagents for cross‐coupling reactions owing to their stability, low toxicity, solubility, and easy accessibility, they are generally inert under typical cross‐coupling conditions. Disclosed herein is a palladium/copper catalytic system that enables the cross‐coupling of trimethyl, triethyl, tert‐butyldimethyl, and triisopropyl aryl silanes with aryl bromides. This process is applicable to the sequential C−H and C−Si bond arylation of thiophenes and the synthesis of poly(thiophene–fluorene)s.

Full Text
Published version (Free)

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 call