Synthetic Route to Chiral Tetrahydroquinoxalines via Ring-Opening of Activated Aziridines
收藏NIAID Data Ecosystem2026-03-07 收录
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A highly regio- and stereoselective route for the synthesis of racemic and nonracemic tetrahydroquinoxalines via the SN2-type ring-opening of activated aziridines with 2-bromoanilines followed by the Pd-catalyzed intramolecular C–N bond formation is described.
创建时间：
2011-11-18
