4.8 Article

Enantioselective Activation of Stable Carboxylate Esters as Enolate Equivalents via N-Heterocyclic Carbene Catalysts

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ORGANIC LETTERS
卷 14, 期 8, 页码 2154-2157

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AMER CHEMICAL SOC
DOI: 10.1021/ol300676w

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  1. Singapore National Research Foundation
  2. Singapore Economic Development Board (EDB)
  3. GlaxoSmithKline (GSK)
  4. Nanyang Technological University (NTU)

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The first N-Heterocyclic Carbene (NHC) mediated activation of stable carboxylate esters to generate enolate intermediates is disclosed. The catalytically generated arylacetic ester enolates undergo enantioselective reactions with alpha,beta-unsaturated imines.

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