Active electropositive α-chlorine: trichloroacetonitrile as an electrophilic chlorination reagent

An inverse-electron C–Cl bond cleavage of Cl 3 CCN under basic conditions to give the chlorine cation, which was used as an unprecedented active electrophilic chlorine source for α-mono- and α-dichlorination of carbonyl compounds.

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2025-01-01
DOI
https://doi.org/10.1039/d5qo00379b
Primary Topic
Oxidative Organic Chemistry Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Active electropositive α-chlorine: trichloroacetonitrile as an electrophilic chlorination reagent

Changming Xu, Bing Zhou, Lei Bai
Organic Chemistry Frontiers
Oxidative Organic Chemistry Reactions
article

Active electropositive α-chlorine: trichloroacetonitrile as an electrophilic chlorination reagent

Changming Xu, Bing Zhou, Lei Bai
article en

Abstract

An inverse-electron C–Cl bond cleavage of Cl 3 CCN under basic conditions to give the chlorine cation, which was used as an unprecedented active electrophilic chlorine source for α-mono- and α-dichlorination of carbonyl compounds.

Organic Chemistry Frontiers
Lanzhou Jiaotong University (CN), Northwest Normal University (CN)
National Natural Science Foundation of China, Natural Science Foundation of Gansu Province
Openalex Percentile: Top 92%
Oxidative Organic Chemistry Reactions
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Active electropositive α-chlorine: trichloroacetonitrile as an electrophilic chlorination reagent — Changming Xu, Bing Zhou, et al. · Organic Chemistry Frontiers (2025) | TGRS Research Map | TGRS