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通过氧化中继在电化学阳极氧化(EAO)条件下获取金π酸反应活性。

Accessing Gold π-Acid Reactivity under Electrochemical Anode Oxidation (EAO) through Oxidation Relay.

作者信息

Shi Xiaodong, Zhang Shuyao, Wei Jingwen, Ye Xiaohan, Perez Angel

机构信息

University of South Florida.

出版信息

Res Sq. 2023 Jul 7:rs.3.rs-3088453. doi: 10.21203/rs.3.rs-3088453/v1.

Abstract

The gold π-acid activation under electrochemical condition is achieved for the first time. While EAO allowing easy access to gold(III) intermediates over alternative chemical oxidation under mild conditions, the reported examples so far limited to coupling reactions due to the rapid AuIII reductive elimination. Using aryl hydrazine-HOTf salt as precursors, the π-activation reaction mode was realized through oxidation relay. Both alkene and alkyne di-functionalization were achieved with excellent functional group compatibility and regioselectivity, which extended the versatility and utility of electrochemical gold redox chemistry for future applications to come.

摘要

首次实现了电化学条件下的金π-酸活化。虽然电化学阳极氧化(EAO)能在温和条件下比其他化学氧化方法更容易地生成金(III)中间体,但由于金(III)的快速还原消除,目前报道的例子仅限于偶联反应。使用芳基肼-三氟甲磺酸(HOTf)盐作为前体,通过氧化接力实现了π-活化反应模式。烯烃和炔烃的双官能团化反应均具有出色的官能团兼容性和区域选择性,这拓展了电化学金氧化还原化学在未来应用中的多功能性和实用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f64a/10350213/aa057daf33de/nihpp-rs3088453v1-f0001.jpg

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