
Precision Chemistry, Год журнала: 2025, Номер unknown
Опубликована: Апрель 10, 2025
Язык: Английский
Precision Chemistry, Год журнала: 2025, Номер unknown
Опубликована: Апрель 10, 2025
Язык: Английский
Angewandte Chemie International Edition, Год журнала: 2025, Номер unknown
Опубликована: Янв. 23, 2025
Despite the increasing interest in radical-based fluoroalkylation techniques, organofluorine compounds bearing partially fluorinated hexafluoroisopropyl group remain extremely scarce due to lack of appropriate reagents. Herein we report an unprecedented photoelectrocatalytic method for C-H hexafluoroisopropylation indoles and tryptophan peptides, utilizing readily available hexafluoro-2-propanol (HFIP) as reagent. In this process, HFIP is converted into radicals, enabling reactions. This study broadens potential applications molecular photoelectrocatalysis, highlighting its capacity enable transformations that are difficult accomplish through traditional electrochemical or photochemical approaches.
Язык: Английский
Процитировано
0Chinese Journal of Chemistry, Год журнала: 2025, Номер unknown
Опубликована: Фев. 24, 2025
Comprehensive Summary Herein we present a novel electrochemical method for the direct decarboxylative phosphorylation of α‐amino acids to phosphonates, key structural element in various biologically active compounds. This bypasses need strong chemical oxidants and 2‐step processes involving preliminary conversions, making it more straightforward synthetic tool. Key success is establish microenvironment on anode surface an acidic solution facilitate selective anodic decarboxylation subsequent C–P formation. The electrosynthetic process continuous flow ensures benign conditions excellent scalability through production with parallel reactors.
Язык: Английский
Процитировано
0Precision Chemistry, Год журнала: 2025, Номер unknown
Опубликована: Апрель 10, 2025
Язык: Английский
Процитировано
0