Investigation on the Stoichiometry of Carbon Dioxide in Isotope-Exchange Reactions with Phenylacetic Acids

被引:5
|
作者
Talbot, Alex [1 ]
Sallustrau, Antoine [1 ]
Goudet, Amelie [1 ]
Taran, Frederic [1 ]
Audisio, Davide [1 ]
机构
[1] Univ Paris Saclay, CEA, Serv Chim Bioorgan & Marquage, DMTS, F-91191 Gif Sur Yvette, France
基金
欧洲研究理事会;
关键词
carbon dioxide; isotope labeling; photoredox catalysis; decarboxylation; carboxylation; TERMINAL ALKYNES; CARBOXYLATION; CO2; DIMETHYLFORMAMIDE; DECARBOXYLATION; COPPER;
D O I
10.1055/s-0040-1720447
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The functionalization of carbon dioxide (CO2) as a C1 building block has attracted enormous attention. Carboxylation reactions, in particular, are of major interest for applications in isotope labeling. Due to the inexpensive nature of CO2, information about its stoichiometric use is generally unavailable in the literature. Because of the rarity and limited availability of CO2 isotopomers, this parameter is of concern for applications in carbon-isotope labeling. We investigated the effects of the stoichiometry of labeled CO2 on carbon isotope exchange of phenyl-acetic acids. Both thermal and photocatalytic procedures were studied, providing insight into product outcome and isotope incorporation. Preliminary results on isotope-dilution effects of carbonate bases in photocatalytic carboxylation reactions have also been obtained.
引用
收藏
页码:171 / 176
页数:6
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