4.8 Article

N-Heterocyclic Carbene-Catalyzed Generation of α,β-Unsaturated Acyl Imidazoliums: Synthesis of Dihydropyranones by their Reaction with Enolates

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JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 131, 期 40, 页码 14176-+

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AMER CHEMICAL SOC
DOI: 10.1021/ja905501z

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  1. ARC [DP0881137]
  2. Australian Research Council [DP0881137] Funding Source: Australian Research Council

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Catalytic generation of alpha,beta-unsaturated acyl imidazolium cations and enolates has been achieved, and their involvement in a Michael addition acylation sequence exploited, to provide a range of dihydropyran ones. alpha,beta-Unsaturated enol esters, or alpha,beta-unsaturated acid fluorides in association with TMS enol ethers, serve as appropriate substrates for this reaction. The transformation can also be achieved enantioselectively using catalysts derived from chiral triazolium salts.

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