Carboxylation of Alkenes with CO2 via Photocatalytic Cleavage of C=C Double Bonds DOI
Qingyuan Meng, Pan‐Feng Yuan

Synlett, Journal Year: 2024, Volume and Issue: 35(17), P. 1937 - 1946

Published: May 14, 2024

Abstract The cleavage of double bonds in alkenes constitutes an integral process converting feedstock materials into high-value synthetic intermediates. Well-known examples such as the oxidative olefins and olefin metathesis only facilitate synthesis oxygen-containing compounds recombination olefins. Therefore, it is appealing to extend C=C bond yield more abundant transformations. Herein, we report a novel photocatalytic approach for deconstructive carboxylation with CO2 carboxylic acids absence transition metals. Compared reported carboxylations during which carbon numbers are typically increased, achieve exchange dioxide one carbons alkene bond, thus providing unchanged when terminal used.

Language: Английский

Visible Light-Induced Carboxylation of Alkenes via Cleavage of Carbon-Carbon Double Bond DOI
Yang Wu, Ji‐Bao Xia

Chinese Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: 44(4), P. 1377 - 1377

Published: Jan. 1, 2024

Language: Английский

Citations

0

Carboxylation of Alkenes with CO2 via Photocatalytic Cleavage of C=C Double Bonds DOI
Qingyuan Meng, Pan‐Feng Yuan

Synlett, Journal Year: 2024, Volume and Issue: 35(17), P. 1937 - 1946

Published: May 14, 2024

Abstract The cleavage of double bonds in alkenes constitutes an integral process converting feedstock materials into high-value synthetic intermediates. Well-known examples such as the oxidative olefins and olefin metathesis only facilitate synthesis oxygen-containing compounds recombination olefins. Therefore, it is appealing to extend C=C bond yield more abundant transformations. Herein, we report a novel photocatalytic approach for deconstructive carboxylation with CO2 carboxylic acids absence transition metals. Compared reported carboxylations during which carbon numbers are typically increased, achieve exchange dioxide one carbons alkene bond, thus providing unchanged when terminal used.

Language: Английский

Citations

0