Nickel-catalyzed arylative cyclization of 1,6-enynes: arylation of unactivated alkene moieties - Archive ouverte HAL
Article Dans Une Revue Organic Chemistry Frontiers Année : 2024

Nickel-catalyzed arylative cyclization of 1,6-enynes: arylation of unactivated alkene moieties

Résumé

We developed catalytic cyclization of 1,6-enynes, whereby an aryl group is introduced at an unactivated alkene moiety. The reaction of a 1,6-enyne with an arylboronic acid in the presence of an Ni(cod)2/P(4-MeOC6H4)3 complex yields a five-membered ring product incorporating an all-carbon quaternary center. Experimental studies and extensive DFT calculations reveal that an Ni(I) species is involved in the catalytic cycle, which is an uncommon pathway involving transmetalation, oxidative cyclization, selective sp3–sp2 carbon–carbon bond formation, and finally hydrolysis.
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Dates et versions

hal-04670086 , version 1 (11-08-2024)

Identifiants

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Jian Gao, Qi Wei, Zeqing Zhang, Zhishan Su, Jialin Ming, et al.. Nickel-catalyzed arylative cyclization of 1,6-enynes: arylation of unactivated alkene moieties. Organic Chemistry Frontiers, 2024, 11 (16), pp.4487-4495. ⟨10.1039/D4QO00784K⟩. ⟨hal-04670086⟩
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