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.

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.

Bibliographic Details
Main Author: Nadi Eleya
Format: Article
Language:English
Published: University of Zakho 2013-06-01
Series:Science Journal of University of Zakho
Subjects:
Online Access:https://sjuoz.uoz.edu.krd/index.php/sjuoz/article/view/94
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spelling doaj-d92c44790a704c5894adfac98137111f2020-11-25T00:42:23Zeng University of ZakhoScience Journal of University of Zakho2663-628X2663-62982013-06-011130030794Synthesis 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.Nadi Eleya0University of ZakhoSuzuki–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.https://sjuoz.uoz.edu.krd/index.php/sjuoz/article/view/94benzophenonesCross-couplingPalladiumRegioselectivity
collection DOAJ
language English
format Article
sources DOAJ
author Nadi Eleya
spellingShingle Nadi Eleya
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
benzophenones
Cross-coupling
Palladium
Regioselectivity
author_facet Nadi Eleya
author_sort Nadi Eleya
title 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.
title_short 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.
title_full 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.
title_fullStr 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.
title_full_unstemmed 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.
title_sort 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.
publisher University of Zakho
series Science Journal of University of Zakho
issn 2663-628X
2663-6298
publishDate 2013-06-01
description 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.
topic benzophenones
Cross-coupling
Palladium
Regioselectivity
url https://sjuoz.uoz.edu.krd/index.php/sjuoz/article/view/94
work_keys_str_mv AT nadieleya synthesisoffunctionalized4aryl23bistrifluoromethanesulfonyloxybenzophenonesbasedonsiteselectivesuzukimiyauracrosscouplingreactionsof234tristrifluoromethanesulfonyloxybenzophenone
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