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Electrochemical Decarboxylative Functionalizations through Carbocation Intermediates

delete2025-10-01
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PRE
AI
F
Fei Lian
Z
Zhoumei Tan *
徐坤 cover
徐坤 (Kun Xu) *
DOI:10.1002/adsc.70137delete
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Abstract

Abstract

En 中文
In contrast to radical-mediated electrochemical decarboxylative couplings, electrochemical decarboxylative functionalizations proceeding through carbocation intermediates (Hofer-Moest pathway) unlock unique reactivity and selectivity. These in situ-generated carbocations can be trapped by diverse nucleophiles or undergo elimination to form alkenes, significantly expanding synthetic versatility. This review systematically surveys advances in electrochemical Hofer-Moest-type reactions since 2019, categorizing transformations by bond-forming events (C-N, C-O, C-P, C-F, C-C, and C=C). Beyond summarizing key breakthroughs, it also provide balanced evaluation of current limitations to delineate the scope and applicability of these methods. Finally, persistent challenges are outlined and future research directions in this emerging field is proposed.
Keywords:
carboxylic acid
electrochemical decarboxylation
electrochemical oxidation
Hofer-Moest reaction

Journal

A
ADVANCED SYNTHESIS & CATALYSIS
IF:
4
Papers:
455
Citations:
0

Organization

C
Chongqing University of Education
Scholars:
658
Papers: 534
Citations: 615
P
pingdingshan university
Scholars:
382
Papers: 130
Citations: 0
B
Beijing University of Technology
Scholars:
2.8W
Papers: 2.1W
Citations: 2.7W
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