4.7 Article

Enantioselective synthesis of 4-aminopyrrolidine-2,4-dicarboxylate derivatives via Ag-catalyzed cycloaddition of azomethine ylides with alkylidene azlactones

期刊

CHEMICAL COMMUNICATIONS
卷 49, 期 41, 页码 4649-4651

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ROYAL SOC CHEMISTRY
DOI: 10.1039/c3cc41663a

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资金

  1. Ministerio de Ciencia e Innovacio'n of Spain (MICINN) [CTQ2009-07791]
  2. Ministerio de Economia y Competitividad (MINECO) [CTQ2012-35790]
  3. CAM (project AVANCAT) [S2009/PPQ-1634]

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A catalytic highly enantioselective silver-DTBM-segphos catalyzed cycloaddition of alpha-iminoesters with alkylidene azlactones is reported. This procedure provides an effective access to 4-aminopyrrolidine- 2,4-dicarboxylate derivatives with high diastereo- and enantioselectivity.

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