Synthesis of Functionalized 4-Aryl-2,3 Bis (Trifluoromethanesulfonyloxy) Benzophenones, Based on Site-Selective Suzuki-Miyaura Cross-Coupling Reactions of 2,3,4-Tris (Trifluoromethanesulfonyloxy) Benzophenone.

Authors

  • Nadi Eleya University of Zakho

Keywords:

benzophenones, Cross-coupling, Palladium, Regioselectivity

Abstract

Suzuki–Miyaura reactions of the tris(triflate) of 2,3,4-benzophenonewith one 1 equivalent of arylboronic acids afforded 4-aryal-2,3-  bis(trifluoromethanesulfonyloxy)benzophenones with very good site selectivity favor of position C4 which is satirically less hindered than position C2.

Author Biography

Nadi Eleya, University of Zakho

Department Of Chemistry, Collage Of Science, Zakho University,Kurdistan – region, Iraq.

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Published

2013-06-30

How to Cite

Eleya, N. (2013). Synthesis of Functionalized 4-Aryl-2,3 Bis (Trifluoromethanesulfonyloxy) Benzophenones, Based on Site-Selective Suzuki-Miyaura Cross-Coupling Reactions of 2,3,4-Tris (Trifluoromethanesulfonyloxy) Benzophenone. Science Journal of University of Zakho, 1(1), 300–307. Retrieved from https://sjuoz.uoz.edu.krd/index.php/sjuoz/article/view/94

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Section

Science Journal of University of Zakho