Alkyl bistriflimidate-mediated electrochemical deaminative functionalization
An efficient electrochemical strategy for the deaminative functionalization of alkyl amines has been described. The alkyl bistriflimidates were readily accessed by the treatment of alkyl amines with trifluoromethanesulfonic anhydride and unprecedentedly employed for C-N bond activation. They can be applied to a range of transformations, including borylation, sulfuration, selenation, sulfonation, Additionally, deaminative esterification and amidation can be performed under catalytic base conditions. The protocol features an undivided cell without the use of transition metal- or photo-catalysts and exhibits high conversion and stability in flow reactors.
Authors
- Shengyang Ni (ORCID: https://orcid.org/0000-0002-6866-8440)
- Xiangzhang Tao (ORCID: https://orcid.org/0000-0001-8859-5771)
- Jiyang Liu (ORCID: https://orcid.org/0000-0003-3699-1646)
- Yi Wang (ORCID: https://orcid.org/0000-0002-8700-7621)
- Jia Xu
- Yi Pan (ORCID: https://orcid.org/0000-0002-1873-2731)
- Hui Shu (ORCID: https://orcid.org/0000-0002-2797-1355)
Institutions
- Collaborative Innovation Center of Advanced Microstructures (CN)
- Nanjing University (CN)
Publication Details
- Journal
- Chemical Science
- Published
- 2024-12-24
- DOI
- https://doi.org/10.1039/d4sc06773h
- Citations
- 4
- Primary Topic
- Radical Photochemical Reactions
- Type
- article
- Field-Weighted Citation Impact
- 1.00
Funders
- National Natural Science Foundation of China