Stereoselective Access to (E)‑1,3-Enynes through Pd/Cu-Catalyzed Alkyne Hydrocarbation of Allenes

PdII and CuI cooperate in catalyzing the alkynes hydrocarbation of allenes (AHA) giving (E)-1,3-enynes with high yields, atom economy, and high regio-/stereoselectivities. We devised new efficient conditions and expanded the substrate scope. Experimental and computational studies support a nonorthod...

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Veröffentlicht in:Organic letters 2019-05, Vol.21 (9), p.3136-3141
Hauptverfasser: Jeanne-Julien, Louis, Masson, Guillaume, Kouoi, Remy, Regazzetti, Anne, Genta-Jouve, Grégory, Gandon, Vincent, Roulland, Emmanuel
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Sprache:eng
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Zusammenfassung:PdII and CuI cooperate in catalyzing the alkynes hydrocarbation of allenes (AHA) giving (E)-1,3-enynes with high yields, atom economy, and high regio-/stereoselectivities. We devised new efficient conditions and expanded the substrate scope. Experimental and computational studies support a nonorthodox PdII/PdIV catalytic cycle involving an oxidative addition triggered by a stereodeterminant H+ transfer. This reaction is leveraged in a new strategy of stereoselective synthesis of 1,3-dienes.
ISSN:1523-7060
1523-7052
DOI:10.1021/acs.orglett.9b00828