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Weilong, Xie
분자활성 촉매반응 연구단
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Copper-Catalyzed Direct C-H Alkylation of Polyfluoroarenes by Using Hydrocarbons as an Alkylating Source

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Title
Copper-Catalyzed Direct C-H Alkylation of Polyfluoroarenes by Using Hydrocarbons as an Alkylating Source
Author(s)
Weilong Xie; Joon Heo; Dongwook Kim; Sukbok Chang
Subject
ELECTRON-DEFICIENT, ; DIRECT ARYLATION, ; ARYL BROMIDES, ; FLUORINE, ; FUNCTIONALIZATION, ; ALLYLATION, ; CHLORIDES, ; BONDS, ; PHARMACEUTICALS, ; ALKENYLATION
Publication Date
2020-04
Journal
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, v.142, no.16, pp.7487 - 7496
Publisher
AMER CHEMICAL SOC
Abstract
Construction of carbon-carbon bonds is one of the most important tools in chemical synthesis. In the previously established cross-coupling reactions, prefunctionalized starting materials were usually employed in the form of aryl or alkyl (pseudo)halides or their metalated derivatives. However, the direct use of arenes and alkanes via a 2-fold oxidative C-H bond activation strategy to access chemoselective C(sp(2))-C(sp(3)) cross-couplings is highly challenging due to the low reactivity of carbon-hydrogen (C-H) bonds and the difficulty in suppressing side reactions such as homocouplings. Herein, we present the new development of a copper-catalyzed cross-dehydrogenative coupling of polyfluoroarenes with alkanes under mild conditions. Relatively weak sp(3) C-H bonds at the benzylic or allylic positions, and nonactivated hydrocarbons could be alkylated by the newly developed catalyst system. A moderate-to-high site selectivity was observed among various C-H bonds present in hydrocarbon reactants, including gaseous feedstocks and complex molecules. Mechanistic information was obtained by performing combined experimental and computational studies to reveal that the copper catalyst plays a dual role in activating both alkane sp(3) C-H bonds and sp(2) polyfluoroarene C-H bonds. It was also suggested that the noncovalent p-p interaction and weak hydrogen bonds formed in situ between the optimal ligand and arene substrates are key to facilitating the current coupling reactions © 2020 American Chemical Society
URI
https://pr.ibs.re.kr/handle/8788114/8660
DOI
10.1021/jacs.0c00169
ISSN
0002-7863
Appears in Collections:
Center for Catalytic Hydrocarbon Functionalizations(분자활성 촉매반응 연구단) > 1. Journal Papers (저널논문)
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