4.7 Article

Homoallyl alcohol as an allylation reagent for termination of the Catellani-Lautens reaction via retro-allylation

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ORGANIC CHEMISTRY FRONTIERS
卷 10, 期 4, 页码 898-904

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ROYAL SOC CHEMISTRY
DOI: 10.1039/d2qo01609e

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A palladium/norbornene-catalyzed ortho-amination/allylation reaction of aryl iodides was developed, which enabled the construction of ortho-aminated allylbenzene using N-benzoyloxyamine as the amination reagent and homoallyl alcohol as the allylation reagent. The reaction exhibited good functional group tolerance and a wide substrate scope.
A palladium/norbornene-catalyzed ortho-amination/allylation of aryl iodides was developed for the construction of ortho-aminated allylbenzene by using N-benzoyloxyamine as the amination reagent and homoallyl alcohol as the allylation reagent. The reaction showed good functional group tolerance and broad substrate scope.

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