Light-induced gold-catalyzed Hiyama arylation: a coupling access to biarylboronates
Organoboron compounds are versatile synthetic building blocks. We herein report a new strategy, a photochemical gold-catalyzed chemo-selective Hiyama arylation of B,Si bifunctionalized reagents with diazonium salts, which is orthogonal to common strategies and therefore a unique tool for synthesis o...
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| Main Authors: | , , , , , , |
|---|---|
| Format: | Article (Journal) |
| Language: | English |
| Published: |
09 October 2018
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| In: |
Angewandte Chemie. International edition
Year: 2018, Volume: 57, Issue: 51, Pages: 16648-16653 |
| ISSN: | 1521-3773 |
| DOI: | 10.1002/anie.201806427 |
| Online Access: | Resolving-System, Volltext: http://dx.doi.org/10.1002/anie.201806427 Verlag, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/anie.201806427 
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| Author Notes: | Jin Xie, Kohei Sekine, Sina Witzel, Petra Krämer, Matthias Rudolph, Frank Rominger, and A. Stephen K. Hashmi |
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| 520 | |a Organoboron compounds are versatile synthetic building blocks. We herein report a new strategy, a photochemical gold-catalyzed chemo-selective Hiyama arylation of B,Si bifunctionalized reagents with diazonium salts, which is orthogonal to common strategies and therefore a unique tool for synthesis of valuable biarylboronates. With this new methodology a wide array of diversely functionalized sp2- and sp3-hybridized biarylboronates were obtained. Notably, the synergism of gold catalysis with copper catalysis or palladium catalysis, allows for one-pot iterative C−X (heteroatom) and C−C couplings for the rapid assembly of several simple fragments to relatively complex molecules. Mechanistic studies indicated that photosensitizer-free conditions were superior to gold/Ru(bpy)3Cl2 dual catalysis. | ||
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| 650 | 4 | |a gold catalysis | |
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| 650 | 4 | |a photochemistry | |
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