Low Pressure Carbonylation of Benzyl Carbonates and Carbamates for Applications in 13C Isotope Labeling and Catalytic CO2 Reduction

被引:2
作者
Day, Craig S. S. [1 ,2 ]
Ton, Stephanie J. J. [1 ,2 ]
Kaussler, Clemens [1 ,2 ]
Hoffmann, Daniel Vronning [1 ,2 ]
Skrydstrup, Troels [1 ,2 ]
机构
[1] Aarhus Univ, Carbon Dioxide Activat Ctr CADIAC, Interdisciplinary Nanosci Ctr iNANO, Gustav Wieds Vej 14, DK-8000 Aarhus, Denmark
[2] Aarhus Univ, Dept Chem, Gustav Wieds Vej 14, DK-8000 Aarhus, Denmark
基金
欧盟地平线“2020”; 新加坡国家研究基金会;
关键词
Carbon Dioxide; Carbonylation; Decarboxylation; Isotope Labeling; Palladium; DECARBOXYLATIVE CARBONYLATION; ALLYLIC CARBONATES; ARYL BROMIDES; PALLADIUM; ACIDS; CARBOXYLATION; CONVERSION; AMINATION; MECHANISM; EXCHANGE;
D O I
10.1002/anie.202308238
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Herein, we report a methodology to access isotopically labeled esters and amides from carbonates and carbamates employing an oxygen deletion strategy. This methodology utilizes a decarboxylative carbonylation approach for isotope labeling with near stoichiometric, ex situ generated C-12, or C-13 carbon monoxide. This reaction is characterized by its broad scope, functional group tolerance, and high yields, which is showcased with the synthesis of structurally complex molecules. A complementary method that operates by the catalytic in situ generation of CO via the reduction of CO2 liberated during decarboxylation has also been developed as a proof-of-concept approach that CO2-derived compounds can be converted to CO-containing frameworks. Mechanistic studies provide insight into the catalytic steps which highlight the impact of ligand choice to overcome challenges associated with low-pressure carbonylation methodologies, along with rational for the development of future methodologies.
引用
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页数:8
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