Abstract
A deeper understanding of reaction mechanisms should lead to improvements in the selectivity of organic electrosynthesis methods. Now, this approach has been used to explain the role of magnesium diacetate in the Ag-electrocatalysed reductive coupling of sp3 organic chlorides with aldehydes or ketones with increased selectivity towards the alcohol product.
Original language | English |
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Pages (from-to) | 115-116 |
Number of pages | 2 |
Journal | Nature Catalysis |
Volume | 7 |
Early online date | 27 Feb 2024 |
DOIs | |
Publication status | Published - Feb 2024 |