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.

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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

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article

Alkyl bistriflimidate-mediated electrochemical deaminative functionalization

Shengyang Ni, Xiangzhang Tao, Jiyang Liu, Yi Wang et al.
4 citations
Chemical Science
Radical Photochemical Reactions
1.00
article

Alkyl bistriflimidate-mediated electrochemical deaminative functionalization

Shengyang Ni, Xiangzhang Tao, Jiyang Liu, Yi Wang, Jia Xu, Yi Pan, Hui Shu
article en
4 citations

Abstract

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.

Chemical ScienceVol. 16(6)
Collaborative Innovation Center of Advanced Microstructures (CN), Nanjing University (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 26%
Radical Photochemical Reactions
1.00
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