4.7 Article

Organocatalytic asymmetric remote aziridination of 2,4-dienals

期刊

CHEMICAL COMMUNICATIONS
卷 49, 期 57, 页码 6382-6384

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ROYAL SOC CHEMISTRY
DOI: 10.1039/c3cc43506g

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资金

  1. Aarhus University, OChem School, FNU
  2. Carlsberg Foundation
  3. South African National Research Foundation
  4. Oppenheimer Memorial Trust

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Highly regio- and stereoselective remote aziridination of 2,4-dienals has been developed, based on a vinylogous iminium-ion-dienamine catalytic cascade reaction. Transformations of the aziridine products into enantio-enriched motifs are also demonstrated. Furthermore, the reaction concept is extended to include enantioselective 1,6-addition of thiols.

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