Electrocarboxylation of CO2 with Organic Substrates: Toward Cathodic Reaction DOI

He Yao,

Mei‐Yan Wang, Chengguang Yue

et al.

Transactions of Tianjin University, Journal Year: 2023, Volume and Issue: 29(4), P. 254 - 274

Published: July 3, 2023

Language: Английский

Electrochemical C−H deuteration of pyridine derivatives with D2O DOI Creative Commons
Zhiwei Zhao,

Ranran Zhang,

Yaowen Liu

et al.

Nature Communications, Journal Year: 2024, Volume and Issue: 15(1)

Published: May 7, 2024

Herein, we develop a straightforward, metal-free, and acid-/base-free electrochemical C4-selective C - H deuteration of pyridine derivatives with economic convenient D

Language: Английский

Citations

15

Recent Advances in Photochemical/Electrochemical Carboxylation of Olefins with CO2 DOI
Qian Wang, Yanwei Wang, Min Liu

et al.

Chinese Journal of Chemistry, Journal Year: 2024, Volume and Issue: 42(18), P. 2249 - 2266

Published: May 15, 2024

Comprehensive Summary CO 2 is an abundant, nontoxic, and renewable C1 feedstock in synthetic chemistry. Direct carboxylation of readily available olefins incorporating regarded as a promising strategy to access high value‐added carboxylic acids well fixation. However, due the thermodynamic stability kinetic inertness difficulty controlling regioselectivity, with still remains challenging. Radical‐type functionalization represented powerful protocol enabled development novel transformations this realm. More recently, advance new technology, such photoredox catalysis renaissance electrochemistry organic synthesis, offered unique chemical reactivities radical precursors provided solutions olefins. This review presents recent advances radical‐type olefins, which has mainly been achieved through photocatalysis electrocatalysis last decade. In article, we provide comprehensive introduction progress, summarize advantages limitations current research, discuss potential outlook for further development. Key Scientists

Language: Английский

Citations

15

Synergistic Effects of Co–Fe Boosts the Transformation of CO2 into C6+ Dicarboxylic Acids up to Gram-Scale under Mild Conditions DOI
Ying Zhang,

Junjun Mao,

Bo Zhang

et al.

ACS Catalysis, Journal Year: 2024, Volume and Issue: 14(3), P. 1459 - 1467

Published: Jan. 13, 2024

Electrochemical carboxylation of 1,3-dienes with carbon dioxide (CO2) is a feasible method to obtain dicarboxylic derivatives, which are important synthetic intermediates polymers and pharmaceuticals. However, due unavoidable byproducts unfriendly conditions, the formation pure acids has been limited. In this work, we report that bimetallic phosphating CoFeP catalyst on nickel foam (CoFeP/NF) served as remarkable electrode, transforms CO2 into multicarbon (C6+) acids. The synergistic effects between Co Fe allow activation mainly, in electron transfer easier proceeded afford radical anion diene, pursuant further formed ultimate carboxylated products. reaction can occur commercial flow cell gram-scale amplification. acid obtained was up 1.08 g at 5 mmol scale 1,3-dienes, illustrating high electrocatalytic activity practical application CoFeP/NF.

Language: Английский

Citations

12

Copper‐Catalyzed C4‐selective Carboxylation of Pyridines with CO2 via Pyridylphosphonium Salts DOI

Shibiao Tang,

Zezhao Liu,

Jiakai Zhang

et al.

Angewandte Chemie International Edition, Journal Year: 2024, Volume and Issue: 63(13)

Published: Feb. 3, 2024

Abstract Pyridine motifs are widespread pharmacophores in many drugs. Installing various substituents through pyridine C−H bond functionalization is significant for new drug design and discovery. Developments of late‐stage reactions enrich the strategies selective pyridines. However, carboxylation pyridines a long‐standing challenge, especially selectively with CO 2 on motifs. Herein, we describe practical method C4−H via one‐pot phosphination copper‐catalyzed resulted phosphonium salts . The reaction conducted under mild conditions compatible multiple active groups several drugs, providing diverse valuable isonicotinic acid compounds, demonstrating application potential this strategy.

Language: Английский

Citations

11

Electro-reductive carboxylation of acyclic C(sp3)–C(sp3) bonds in aromatic hydrocarbons with CO2 DOI

Chuan‐Kun Ran,

Quan Qu,

Yang-Yi Tao

et al.

Science China Chemistry, Journal Year: 2024, Volume and Issue: 67(10), P. 3366 - 3372

Published: Aug. 16, 2024

Language: Английский

Citations

10

An electrocatalytic mono-functionalization of alkenes towards alkenyl selenium sulfonates DOI

Zhiheng Zhao,

Hongyan Yan,

Lijun Gu

et al.

Chemical Communications, Journal Year: 2025, Volume and Issue: unknown

Published: Jan. 1, 2025

In this study, a straightforward and environmentally benign electrochemical mono-functionalization of alkenes has been established for the synthesis alkenyl selenium sulfonates using elemental as source.

Language: Английский

Citations

1

Organo-mediator enabled electrochemical transformations DOI
Wei-Mei Zeng, Yanwei Wang,

Chunhui Peng

et al.

Chemical Society Reviews, Journal Year: 2025, Volume and Issue: unknown

Published: Jan. 1, 2025

This review highlights organo-mediators that enable electrochemical reactions via outer-sphere electron transfer (ET), offering advantages such as availability, tunability, and simplified post-processing compared to direct electrolysis.

Language: Английский

Citations

1

Metal-free electrochemical dihydroxylation of unactivated alkenes DOI Creative Commons
Min Liu, Tian Feng, Yanwei Wang

et al.

Nature Communications, Journal Year: 2023, Volume and Issue: 14(1)

Published: Oct. 13, 2023

Herein, a metal-free electrochemical dihydroxylation of unactivated alkenes is described. The transformation proceeds smoothly under mild conditions with broad range alkenes, providing valuable and versatile dihydroxylated products in moderate to good yields without the addition costly transition metals stoichiometric amounts chemical oxidants. Moreover, this method can be applied natural pharmaceutical derivatives, further demonstrating its synthetic utility. Mechanistic studies have revealed that iodohydrin epoxide intermediate are formed during reaction process.

Language: Английский

Citations

22

Electroreductive Cross‐Electrophile Coupling of Aziridines and Aryl Bromides DOI

Guoqing Yang,

Yanwei Wang, Youai Qiu

et al.

Chemistry - A European Journal, Journal Year: 2023, Volume and Issue: 29(36)

Published: April 18, 2023

Herein, a nickela-electrocatalyzed cross-electrophile coupling of readily available aryl aziridines and bromides under mild sustainable electrochemical conditions to access synthetic useful β-arylethylamines is developed. This protocol characterized by its exquisite chemo- regioselectivity, broad substrate scope good functional group compatibility. Mechanistic studies confirmed that the regioselectivity reactivity observed are result electro-induced ring-opening electroreductive generate benzyl radical intermediate as active species. Furthermore, this strategy also enables cross-coupling with CO2 β-amino acids conditions.

Language: Английский

Citations

18

Electrochemical conversion of organic compounds and inorganic small molecules DOI

Wei-Mei Zeng,

Youai Qiu

Science China Chemistry, Journal Year: 2024, Volume and Issue: 67(10), P. 3223 - 3246

Published: July 9, 2024

Language: Английский

Citations

7