...
首页> 外文期刊>Hwahak konghak >Synthesis of Enantiopure Epoxide Compounds Using Dimeric Chiral Salen Catalyst
【24h】

Synthesis of Enantiopure Epoxide Compounds Using Dimeric Chiral Salen Catalyst

机译:二聚手性Salen催化剂合成对映体纯环氧化合物

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

The stereoselective synthesis of chiral terminal epoxide is of immense academic and industrial interest due to their utility as versatile starting materials as well as chiral intermediates.In this review,we investigate the research and development trend in the asymmetric ring opening reactions using cobalt salen catalysts.Hydro-lytic kinetic resolution(HKR)technology is the very prominent way to prepare optically pure terminal epoxides among available methods.We have synthesized homogeneous and heterogeneous chiral dinuclear salen complexes and demonstrated their catalytic activity and selectivity for the asymmetric ring opening of terminal epoxides with variety of nucleophiles and for asymmetric cyclization to prepare optically pure terminal epoxides in one step.The resolved ring opened product combined with ring closing in the presence of base and catalyst afforded the enantioriched terminal epoxides in quantitaive yield.Potentially,these catalysts are using on an industrial scale to produce chiral intermediates.The experimental results of HKR technology applied to the synthesis of various chiral compounds are presented in this paper.
机译:由于其作为通用原料和手性中间体的实用性,手性末端环氧化物的立体选择性合成具有广泛的学术和工业兴趣。在本文中,我们研究了使用钴-赛伦催化剂的不对称开环反应的研究和发展趋势。水解动力学拆分(HKR)技术是制备光学纯末端环氧化物的最主要方法。我们已经合成了均相和非均相的手性双核Salen配合物,并证明了它们对末端环氧化物不对称开环的催化活性和选择性各种亲核试剂并通过不对称环化一步制备光学纯的末端环氧化物。在碱和催化剂的存在下,拆分的开环产物与闭环相结合,可以定量收率得到对映异构的末端环氧化物。工业规模本文介绍了HKR技术应用于合成各种手性化合物的实验结果。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号