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.
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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 |
_version_ |
1725282909031497728 |