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A low-cost electrochemical thio- and selenocyanation strategy for electron-rich arenes under catalyst- and oxidant-free conditions
A low-cost and efficient thio- and selenocyanation strategy for electron-rich arenes has been developed under constant-current electrolytic conditions in an undivided cell. This strategy is versatile for various (hetero)aromatic compounds such as indole, pyrrole, aniline and anisole under mild condi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9081088/ https://www.ncbi.nlm.nih.gov/pubmed/35541747 http://dx.doi.org/10.1039/c8ra04407d |
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author | Zhang, Xing Wang, Chenguang Jiang, Hong Sun, Linhao |
author_facet | Zhang, Xing Wang, Chenguang Jiang, Hong Sun, Linhao |
author_sort | Zhang, Xing |
collection | PubMed |
description | A low-cost and efficient thio- and selenocyanation strategy for electron-rich arenes has been developed under constant-current electrolytic conditions in an undivided cell. This strategy is versatile for various (hetero)aromatic compounds such as indole, pyrrole, aniline and anisole under mild conditions without any catalyst or oxidant. Readily available salts NH(4)SCN and KSeCN are employed respectively as the sole reagent. |
format | Online Article Text |
id | pubmed-9081088 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90810882022-05-09 A low-cost electrochemical thio- and selenocyanation strategy for electron-rich arenes under catalyst- and oxidant-free conditions Zhang, Xing Wang, Chenguang Jiang, Hong Sun, Linhao RSC Adv Chemistry A low-cost and efficient thio- and selenocyanation strategy for electron-rich arenes has been developed under constant-current electrolytic conditions in an undivided cell. This strategy is versatile for various (hetero)aromatic compounds such as indole, pyrrole, aniline and anisole under mild conditions without any catalyst or oxidant. Readily available salts NH(4)SCN and KSeCN are employed respectively as the sole reagent. The Royal Society of Chemistry 2018-06-14 /pmc/articles/PMC9081088/ /pubmed/35541747 http://dx.doi.org/10.1039/c8ra04407d Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Zhang, Xing Wang, Chenguang Jiang, Hong Sun, Linhao A low-cost electrochemical thio- and selenocyanation strategy for electron-rich arenes under catalyst- and oxidant-free conditions |
title | A low-cost electrochemical thio- and selenocyanation strategy for electron-rich arenes under catalyst- and oxidant-free conditions |
title_full | A low-cost electrochemical thio- and selenocyanation strategy for electron-rich arenes under catalyst- and oxidant-free conditions |
title_fullStr | A low-cost electrochemical thio- and selenocyanation strategy for electron-rich arenes under catalyst- and oxidant-free conditions |
title_full_unstemmed | A low-cost electrochemical thio- and selenocyanation strategy for electron-rich arenes under catalyst- and oxidant-free conditions |
title_short | A low-cost electrochemical thio- and selenocyanation strategy for electron-rich arenes under catalyst- and oxidant-free conditions |
title_sort | low-cost electrochemical thio- and selenocyanation strategy for electron-rich arenes under catalyst- and oxidant-free conditions |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9081088/ https://www.ncbi.nlm.nih.gov/pubmed/35541747 http://dx.doi.org/10.1039/c8ra04407d |
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