4.8 Article

Copper-Catalyzed Enantioselective Intramolecular N-Arylation, an Efficient Method for Kinetic Resolutions

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ORGANIC LETTERS
卷 15, 期 14, 页码 3598-3601

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AMER CHEMICAL SOC
DOI: 10.1021/ol401449b

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  1. CAS
  2. National Natural Science Foundation [21272234]
  3. National S&T Major Special Project on Major New Drug Innovation [2011ZX09102-010]
  4. Guangdong Natural Science Foundation [S2011010003705]

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For the first time, copper-catalyzed intramolecular N-arylation was successfully applied to the kinetic resolution strategy. Under the catalysis of Cul-BINOL derived ligands, the kinetic resolution of rac-2-amino-3-(2-iodoaryl)propionates and rac-2-amino-4-(2-iodoaryl)butanoates afforded chiral intramolecular coupling products and recovered the starting materials in high enantioselectivity (s factors up to 245).

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