Thiolate photocatalysis enables radical borylation of reductively inert aryl electrophiles
The facile installation of functionalities to aromatic compounds via chemical activation of inert carbon-heteroatom bonds is a challenging task. In this issue of Chem, König and co-workers disclose a photocatalytic protocol for the radical borylation of reductively inert aryl electrophiles, such as...
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| Main Authors: | , |
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| Other Authors: | |
| Format: | Article |
| Language: | English |
| Published: |
2022
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| Subjects: | |
| Online Access: | https://hdl.handle.net/10356/157069 |
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| Institution: | Nanyang Technological University |
| Language: | English |
| Summary: | The facile installation of functionalities to aromatic compounds via chemical activation of inert carbon-heteroatom bonds is a challenging task. In this issue of Chem, König and co-workers disclose a photocatalytic protocol for the radical borylation of reductively inert aryl electrophiles, such as aryl fluorides and aryl carbonates, by using simple thiolate salts as a catalyst. |
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