Nickel-Catalyzed Electrochemical Cyclizative Carboxylation of Alkene-Tethered Carbamoyl Chlorides with Carbon Dioxide

Lin-Lin Wang; Xiao-Fei Liu; He Wang; Li Tao; Jian Huang; Wei-Min Ren; Xiao-Bing Lu; Wen-Zhen Zhang

doi:10.1055/s-0041-1738439

Synthesis, Inhaltsverzeichnis

Synthesis 2023; 55(18): 2951-2958
DOI: 10.1055/s-0041-1738439

paper

Special Issue Electrochemical Organic Synthesis

Nickel-Catalyzed Electrochemical Cyclizative Carboxylation of Alkene-Tethered Carbamoyl Chlorides with Carbon Dioxide

Lin-Lin Wang‡

,

Xiao-Fei Liu‡

,

He Wang

,

Li Tao

,

Jian Huang

,

Wei-Min Ren

,

Xiao-Bing Lu

,

Wen-Zhen Zhang ∗

Abstract

Alle Artikel dieser Rubrik

Abstract

Nickel-catalyzed electrochemical cyclizative carboxylation of alkene-tethered carbamoyl chlorides with atmospheric carbon dioxide in an undivided cell under simple constant current conditions is reported. This reaction is conducted with high efficiency under mild conditions, providing a convenient and green access to valuable 2-oxoindolin-3-ylacetic acids and 2-oxo-tetrahydroquinoline-4-carboxylic acids.

Key words

carbon dioxide - cyclizative carboxylation - organic electrosynthesis - nickel catalysis - carbamoyl chlorides

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