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.
Article Sidebar
Published:
2013-06-30
Keywords:
benzophenones, Cross-coupling, Palladium, Regioselectivity
Main Article Content
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.
Downloads
Download data is not yet available.
Article Details
Section
Science Journal of University of Zakho
This work is licensed under a Creative Commons Attribution 4.0 International License.
Authors who publish with this journal agree to the following terms:
- Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution License [CC BY-NC-SA 4.0] that allows others to share the work with an acknowledgment of the work's authorship and initial publication in this journal.
- Authors are able to enter into separate, additional contractual arrangements for the non-exclusive distribution of the journal's published version of the work, with an acknowledgment of its initial publication in this journal.
- Authors are permitted and encouraged to post their work online.
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. https://www.stest.uoz.edu.krd/index.php/sjuoz/article/view/94