首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >Lewis base catalysis of bromo- and iodolactonization,and cycloetherification
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Lewis base catalysis of bromo- and iodolactonization,and cycloetherification

机译:Lewis碱催化溴代和碘代内酯化,以及环醚化

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摘要

Lewis base catalyzed bromo- and iodolactonization reactions have been developed and the effects of catalyst structure on rate and cyclization selectivity have been systematically explored. The effects of substrate structure on halolactonization reactions and the interaction of those effects with the effects of catalyst structure have been investigated, leading to synthetically useful improvements in cyclization selectivity. The knowledge acquired was applied to the development of Lewis base catalyzed bromo-and iodocycloetherification reactions. The ability of some of the surveyed catalysts to influence the cyclization selectivity of halolactonization reactions demonstrates their presence in the transition structure of the product-determining cyclization step. This observation implies that chiral derivatives of these catalysts have the potential to provide enantioenriched products regardless of the rates or mechanisms of halonium ion racemization.
机译:已经开发了路易斯碱催化的溴代和碘代内酯化反应,并且系统地探索了催化剂结构对速率和环化选择性的影响。已经研究了底物结构对卤代内酯化反应的影响以及这些作用与催化剂结构的影响之间的相互作用,从而在环化选择性方面取得了合成上有用的改进。获得的知识可用于开发Lewis碱催化的溴代和碘代环醚化反应。一些被调查的催化剂影响卤代内酯化反应的环化选择性的能力证明了它们存在于决定产物的环化步骤的过渡结构中。该观察结果表明,这些催化剂的手性衍生物具有提供对映体富集产物的潜力,而与ha离子外消旋的速率或机理无关。

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