| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5211953 | Tetrahedron | 2017 | 6 Pages |
Abstract
NHC-Pd-PEPPSI complexes with bulky benzyladamantyl substituted N-heterocyclic carbenes (NHC) were synthesized and characterized by NMR, HRMS, and micro analysis. These complexes were then used for Suzuki-Miyaura coupling reactions between aryl bromides and phenylboronic acid. With low catalyst loading, all synthesized complexes rapidly catalyzed the Suzuki-Miyaura cross-coupling reaction in i-PrOH/water (1:3 v/v) at room temperature in air. All palladium compounds were stable and had high catalytic activity for the Suzuki-Miyaura coupling reaction.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Zineb Imene Dehimat, Aziz PaÅahan, Dahmane Tebbani, Sedat YaÅar, Ä°smail Ãzdemir,