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Cationic Micelle-catalyzed Ring-Opening Reactions of Aziridines with Thiols in Water

Cationic Micelle-catalyzed Ring-Opening Reactions of Aziridines with Thiols in Water
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摘要 一个有效、实际的方法在温和条件下面在水里与各种各样的 thiols 为 N-tosylaziridines 的戒指洞反应被描述。各种各样的表面活化剂被评估了优化反应。在最佳的条件下面,这些反应产生了相应氨基的硫化物在对优秀收益好。 An efficient and practical method is described for the ring-opening reactions of N-tosylaziridines with various thiols in water under mild conditions. Various surfactants have been evaluated to optimize the reactions. Under optimal conditions, these reactions gave rise to the corresponding β-amino sulfides in good to excellent yields.
出处 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2011年第3期499-503,共5页 中国化学(英文版)
基金 Project supported by the National Natural Science Foundation of China (Nos. '20862009, 20962010), Jiangxi Educational Committee (No. G J J10386) and the National Natural Science Foundation of Jiangxi Province (No. 2008GQH0026).
关键词 开环反应 胶束催化 硫醇 阳离子 吖啶 表面活性剂 温和条件 pyridine-N-oxide, ring-opening reaction, N-tosylaziridine, thiol, β-amino sulfide
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