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Suzuki-Miyaura coupling reaction of aryl chlorides using di(2,6-dimethylmorpholino)phenylphosphine as ligand |
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| Authors: | Su-Dong Cho Heung-seop Yim Jin-Kook Lee |
| Institution: | a Department of Polymer Science and Engineering, Pusan National University, Busan 609-735, Republic of Korea b Department of Chemistry and Graduate School for Molecular Materials and Nanochemistry, Gyeongsang National University, Jinju 660-701, Republic of Korea c Center for Plastic Information System, Pusan National University, Busan 609-735, Republic of Korea d Department of Chemistry and Environmental Biotechnology National Core Research Center, Graduate School for Molecular Materials and Nanochemistry, Gyeongsang National University, Jinju 660-701, Republic of Korea |
| Abstract: | Suzuki-Miyaura coupling was achieved on a variety of aryl chlorides by using di(2,6-dimethylmorpholino)phenylphosphine (L1) as a bulky electron-rich monoaryl phosphine ligand. We report the couplings of various chlorobenzenes and heteroaryl chlorides. |
| Keywords: | Suzuki-Miyaura coupling Pd-catalyzed coupling of aryl chlorides PN2 ligand C-C coupling reaction |
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