A Nickel(II)‐Mediated Thiocarbonylation Strategy for Carbon Isotope Labeling of Aliphatic Carboxamides

Author(s):  
Simon S. Pedersen ◽  
Aske S. Donslund ◽  
Jesper H. Mikkelsen ◽  
Oskar S. Bakholm ◽  
Florian Papp ◽  
...  
2021 ◽  
Vol 27 (24) ◽  
pp. 6998-6998
Author(s):  
Simon S. Pedersen ◽  
Aske S. Donslund ◽  
Jesper H. Mikkelsen ◽  
Oskar S. Bakholm ◽  
Florian Papp ◽  
...  
Keyword(s):  

Carbon ◽  
2021 ◽  
Author(s):  
Pingping Zhuang ◽  
Jing Liu ◽  
Junjie Huang ◽  
Chao Dou ◽  
Weiwei Cai ◽  
...  

2020 ◽  
Vol 56 (78) ◽  
pp. 11677-11680
Author(s):  
Antonio Del Vecchio ◽  
Alex Talbot ◽  
Fabien Caillé ◽  
Arnaud Chevalier ◽  
Antoine Sallustrau ◽  
...  

A procedure which allows labelling cyclic carbamates with all carbon isotopes has been developed. This protocol valorizes carbon dioxide, the universal building block for radiolabeling. A series of pharmaceuticals were obtained and a disconnection/reconnection strategy was implemented.


Synlett ◽  
2021 ◽  
Author(s):  
Davide Audisio ◽  
Alex Talbot ◽  
Antoine Sallustrau ◽  
Amélie Goudet ◽  
Frédéric Taran

AbstractThe 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 phenyl­acetic 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.


Trees ◽  
2010 ◽  
Vol 25 (2) ◽  
pp. 187-198 ◽  
Author(s):  
Thorsten E. E. Grams ◽  
Herbert Werner ◽  
Daniel Kuptz ◽  
Wilma Ritter ◽  
Frank Fleischmann ◽  
...  

1990 ◽  
Vol 82 (1) ◽  
pp. 18-21 ◽  
Author(s):  
Tony J. Svejcar ◽  
Thomas W. Boutton ◽  
James D. Trent

2021 ◽  
Author(s):  
Victor Babin ◽  
Antoine Sallustrau ◽  
Olivier Loreau ◽  
Fabien Caillé ◽  
Amélie Goudet ◽  
...  

Carbon isotope labeling is a traceless technology, which allows tracking the fate of organic compounds either in the environment or in living organisms. Despite recent advances in the field, the development of robust and general technologies remains a significant task. This full article reports on a general approach to label urea derivatives with all carbon isotopes, including <sup>14</sup>C and <sup>11</sup>C. Based on a Staudinger aza-Wittig sequence, it provides access to all aliphatic/aromatic urea combinations as well as to semicarbazides, sulfonylureas, hydroxyl ureas, and simple terminal ureas. A de-risking approach was developed to evaluate the robustness of the reaction. This technology is based on [<sup>14</sup>C]CO<sub>2</sub> screening that allowed to investigate the tolerance of the procedure with most representative heterocycles and functional groups found in FDA approved drugs.


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