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Challenging cross couplings, in water, aided by iodination of (hetero)aromatic bromides
Palladium-catalyzed reactions that involve functionalized substrates are oftentimes problematic. Those involving aryl or heteroaryl bromides that are either resistant to, or inefficient in such couplings present challenges that are difficult to overcome and may require development of an entirely new...
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Published in: | Chemical science (Cambridge) 2023-11, Vol.14 (46), p.1353-1357 |
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Main Authors: | , , |
Format: | Article |
Language: | |
Online Access: | Get full text |
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Summary: | Palladium-catalyzed reactions that involve functionalized substrates are oftentimes problematic. Those involving aryl or heteroaryl bromides that are either resistant to, or inefficient in such couplings present challenges that are difficult to overcome and may require development of an entirely new route, or worse, no opportunity to install the desired group using a standard coupling strategy. In this report, we describe a solution that allows for the
in situ
conversion of such bromo educts to transient iodide derivatives that can be made and used under environmentally responsible conditions, for subsequent reactions to highly functionalized, complex targets.
Palladium-catalyzed reactions that involve functionalized substrates are oftentimes problematic. An initial Br-to-I conversion followed by an immediate cross coupling may allow for the targeted C-C bonds to be obtained. |
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ISSN: | 2041-6520 2041-6539 |
DOI: | 10.1039/d3sc04199a |