| Literature DB >> 28884491 |
Gregory A Price1, Abbas Hassan1,2, Nalin Chandrasoma1, Andrew R Bogdan3, Stevan W Djuric3, Michael G Organ1,4.
Abstract
A silica-supported precatalyst, Pd-PEPPSI-IPent-SiO2 , has been prepared and evaluated for its proficiency in the Negishi cross-coupling of hindered and electronically deactivated coupling partners. The precatalyst Pd-PEPPSI-IPent loaded onto packed bed columns shows high catalytic activity for the room-temperature coupling of deactivated/hindered biaryl partners. Also for the first time, the flowed Csp3 -Csp2 coupling of secondary alkylzinc reagents to (hetero)aromatics has been achieved with high selectivity with Pd-PEPPSI-IPent-SiO2 . These couplings required residence times as short as 3 minutes to effect completion of these challenging transformations with excellent selectivity for the nonrearranged product.Entities:
Keywords: N-heterocyclic carbenes; arenes; cross-coupling; flow chemistry; palladium
Year: 2017 PMID: 28884491 DOI: 10.1002/anie.201708598
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336