Kittisak YasamutJira JongcharoenkamolSomsak RuchirawatPoonsakdi PloypradithChulabhorn Research InstituteMahidol UniversityChulabhorn Graduate InstituteThailand Ministry of Education2018-12-112019-03-142018-12-112019-03-142016-01-01Tetrahedron. Vol.72, No.40 (2016), 5994-600014645416004040202-s2.0-84986286556https://repository.li.mahidol.ac.th/handle/20.500.14594/43319© 2016 Elsevier Ltd A novel Cu(0)-Cu(I)-mediated Caryl-CarylUllmann coupling has been successfully developed. The use of Cu(I) salts allowed the reactions to proceed under relatively mild conditions (65 °C in DMSO for 15–72 h). The developed method was compatible with a relatively wide range of functional groups simultaneously present on the aromatic ring of different electronic nature. The aryl halides with an electron-withdrawing group ortho to the halide or an electron-donating group meta or para to the halide furnished the corresponding products in good to excellent yields (up to 98%).Mahidol UniversityBiochemistry, Genetics and Molecular BiologyChemistryArticleSCOPUS10.1016/j.tet.2016.07.063