Diazonium Salts as Nitrogen-Based Lewis Acids
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| Publication date | 05-2019 |
| Journal | Synlett |
| Volume | Issue number | 30 | 8 |
| Pages (from-to) | 875-884 |
| Number of pages | 10 |
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| Abstract |
Aryldiazonium salts are widely used in many organic transformations with displacement of N2 or through addition to the terminal nitrogen. Such aryldiazonium salts can be viewed as N-based Lewis acids that can react with Lewis bases to synthesize a wide variety of azo compounds. Additionally, diazonium salts are known to undergo single-electron transfer and release N2, forming an aryl radical, which results in different reactivity. Herein, we provide a concise overview of the reactivity of aryldiazonium salts undergoing classical donor-acceptor reactivity or single-electron transfer.
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| Document type | Article |
| Language | English |
| Published at | https://doi.org/10.1055/s-0037-1612109 |
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Diazonium Salts
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