Electrochemical aerobic Wacker-type oxygenation of triaryl substituted alkenes to 1,2,2-triarylethanones-Reference-Cited by-同舟云学术

Electrochemical aerobic Wacker-type oxygenation of triaryl substituted alkenes to 1,2,2-triarylethanones

Published:2024 Issue:22 Volume:60 Page:3035-3038
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Zhang Zhou¹,Li Jin²,Cai Zhiwei³,Kang Songyao³,Wang Jian²,Cui Yue²,Han Siyuan²,Sheng Lei³^ORCID,Yin Qing³,Dai Ang³,Zhao Weining³^ORCID,Zhao Fangyuan¹

Affiliation:

1. School of Chemical Engineering & Technology, China University of Mining and Technology, Xuzhou 221116, Jiangsu, P. R. China

2. Faculty of Chemical Engineering, Huaiyin Institute of Technology, Huai’an 223003, Jiangsu, P. R. China

3. College of Pharmacy, Shenzhen Technology University, Shenzhen 518118, Guangdong, P. R. China

Abstract

An electrochemical oxygenation approach to obtain 1,2,2-triarylethanones represents the first expansion of Wacker-type oxidation substrate scope to triaryl-substituted alkenes.

Funder

National Natural Science Foundation of China

Shenzhen Technology University

Natural Science Foundation of Jiangsu Province

Shuangchuang Program of Jiangsu Province

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/CC/D3CC05770D

Reference28 articles.

1. Metal-Catalyzed α-Arylation of Carbonyl and Related Molecules: Novel Trends in CC Bond Formation by CH Bond Functionalization

2. Direct Copper-Catalyzed α-Arylation of Benzyl Phenyl Ketones with Aryl Iodides: Route towards Tamoxifen

3. Aqueous α-Arylation of Mono- and Diarylethanone Enolates at Low Catalyst Loading

4. Palladium-Catalyzed Denitrative α-Arylation of Ketones with Nitroarenes

5. Transition Metal‐Free Aroylation of Diarylmethanes withN‐Bn‐N‐Boc Arylamides andN‐Acylpyrroles