Preparation of Dienyl Boronates by Tandem Ene–Yne Metathesis/Dienyl Isomerization: Ready Access to Diene Building Blocks for the Synthesis of Polyenes

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 isom...

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Veröffentlicht in:Journal of organic chemistry 2022-11, Vol.87 (21), p.14078-14092
Hauptverfasser: Rohde, Laurence N., Diver, Steven T.
Format: Artikel
Sprache:eng
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Zusammenfassung: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.
ISSN:0022-3263
1520-6904
DOI:10.1021/acs.joc.2c01678