Abstract
The quest to find milder and more sustainable methods to generate highly reactive, carbon-centred intermediates has led to a resurgence of interest in radical chemistry. In particular, carboxylic acids are seen as attractive radical precursors due their availability, low cost, diversity, and sustainability. Moreover, the corresponding nucleophilic carbon-radical can be easily accessed through a favourable radical decarboxylation process, extruding CO2 as a traceless by-product. This review summarizes the recent progress on using carboxylic acids directly as convenient radical precursors for the formation of carbon-carbon bonds via the 1,4-radical conjugate addition (Giese) reaction.
| Original language | English |
|---|---|
| Pages (from-to) | 1415-1453 |
| Number of pages | 39 |
| Journal | Chemical Society Reviews |
| Volume | 51 |
| Issue number | 4 |
| Early online date | 31 Jan 2022 |
| DOIs | |
| Publication status | Published - 21 Feb 2022 |
ASJC Scopus subject areas
- General Chemistry
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