Catalyst-free electrochemical dearomatization of pyridine derivatives

We demonstrated herein an electrochemical dearomatizative alkylation of Katritzky salts, wherein Katritzky salts were harnessed as both radical acceptors and donors. A wide range of privileged dihydropyridine scaffolds was constructed with good to excellent yields. Cyclic voltammetry (CV) and electr...

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Published inGreen synthesis and catalysis Vol. 5; no. 2; pp. 136 - 139
Main Authors Wang, Kui, Tian, Yingjun, Li, Baoying, Wang, Ling, Gao, Wei, Jia, Xiaofei, Wang, Ruiming, Zhu, Yanping, Chen, Jianbin
Format Journal Article
LanguageEnglish
Published Elsevier B.V 01.05.2024
KeAi Communications Co. Ltd
Subjects
Dearomatization
Dihydropyridine
Electrosynthesis
Katritzky salts
Dearomatization
Electrosynthesis
Dihydropyridine
Katritzky salts
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Abstract We demonstrated herein an electrochemical dearomatizative alkylation of Katritzky salts, wherein Katritzky salts were harnessed as both radical acceptors and donors. A wide range of privileged dihydropyridine scaffolds was constructed with good to excellent yields. Cyclic voltammetry (CV) and electron paramagnetic resonance (EPR) results confirmed the key intermediates-dihydropyridine radicals and gram-scale reaction highlighted the practical and sustainable feature of the newly developed protocol. An electrochemical dearomatizative alkylation of Katritzky salts was described, accomplishing the privileged dihydropyridine scaffolds in excellent yields. EPR and CV determination corroborate the dihydropyridine radicals via the dearomatization. [Display omitted]
AbstractList We demonstrated herein an electrochemical dearomatizative alkylation of Katritzky salts, wherein Katritzky salts were harnessed as both radical acceptors and donors. A wide range of privileged dihydropyridine scaffolds was constructed with good to excellent yields. Cyclic voltammetry (CV) and electron paramagnetic resonance (EPR) results confirmed the key intermediates-dihydropyridine radicals and gram-scale reaction highlighted the practical and sustainable feature of the newly developed protocol. An electrochemical dearomatizative alkylation of Katritzky salts was described, accomplishing the privileged dihydropyridine scaffolds in excellent yields. EPR and CV determination corroborate the dihydropyridine radicals via the dearomatization. [Display omitted]
We demonstrated herein an electrochemical dearomatizative alkylation of Katritzky salts, wherein Katritzky salts were harnessed as both radical acceptors and donors. A wide range of privileged dihydropyridine scaffolds was constructed with good to excellent yields. Cyclic voltammetry (CV) and electron paramagnetic resonance (EPR) results confirmed the key intermediates-dihydropyridine radicals and gram-scale reaction highlighted the practical and sustainable feature of the newly developed protocol.
Author Zhu, Yanping
Wang, Ruiming
Chen, Jianbin
Gao, Wei
Wang, Kui
Jia, Xiaofei
Tian, Yingjun
Li, Baoying
Wang, Ling
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Issue 2
Keywords Dearomatization
Electrosynthesis
Dihydropyridine
Katritzky salts
Language English
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Snippet We demonstrated herein an electrochemical dearomatizative alkylation of Katritzky salts, wherein Katritzky salts were harnessed as both radical acceptors and...
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SubjectTerms Dearomatization
Dihydropyridine
Electrosynthesis
Katritzky salts
Title Catalyst-free electrochemical dearomatization of pyridine derivatives
URI https://dx.doi.org/10.1016/j.gresc.2022.06.006
https://doaj.org/article/69c706bd863c4ce7bee89439edbedf1b
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