Abstract
The ene-yne metathesis of alkenyl boronates with terminal alkynes is reported. These challenging metatheses were accomplished using a Grubbs catalyst bearing the cyclic alkyl amino carbene (CAAC) ligand, whereas N-heterocyclic carbene (NHC) derived catalysts gave lower yields. Subsequent dienyl isomerization via a cobalt-catalyzed hydrogen atom transfer (HAT) furnished the more substituted dienyl boronate with high EE/EZ ratios. Finally, the resulting dienyl boronate products were successfully used in Suzuki-Miyaura cross-coupling reactions and in a Diels-Alder cycloaddition.
| Original language | English |
|---|---|
| Pages (from-to) | 14078-14092 |
| Number of pages | 15 |
| Journal | Journal of Organic Chemistry |
| Volume | 87 |
| Issue number | 21 |
| DOIs | |
| State | Published - Nov 4 2022 |
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