Palladium-catalysed directed remote -C-H functionalization of arenes using a cyclopentenyl-pyridyl template

Achieving positionally selective distal C-H functionalization remains a fundamental and longstanding challenge in the field of C-H activation. The directing template strategy has emerged as a promising solution to this problem. Herein, we disclose the development of a novel non-aromatic meta -select...

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Veröffentlicht in:New journal of chemistry 2024-08, Vol.48 (34), p.15172-15178
Hauptverfasser: Huang, Jun, Tang, Jinghong, Yan, Yifei, Liu, Zelin, He, Siquan, Jin, Zhong
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container_end_page 15178
container_issue 34
container_start_page 15172
container_title New journal of chemistry
container_volume 48
creator Huang, Jun
Tang, Jinghong
Yan, Yifei
Liu, Zelin
He, Siquan
Jin, Zhong
description Achieving positionally selective distal C-H functionalization remains a fundamental and longstanding challenge in the field of C-H activation. The directing template strategy has emerged as a promising solution to this problem. Herein, we disclose the development of a novel non-aromatic meta -selective directing template, which showed eminent reactivity and site-selectivity in palladium-catalyzed remote meta -C-H olefination, deuteration and acetoxylation of benzyl alcohols. Highly meta -selective C-H olefination, deuteration and acetoxylation of benzyl alcohols were realized by applying a practical directing template featuring a non-aromatic cyclopentenyl-pyridine scaffold.
doi_str_mv 10.1039/d4nj02945c
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source Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection
title Palladium-catalysed directed remote -C-H functionalization of arenes using a cyclopentenyl-pyridyl template
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