手性硒酸盐-双酚配合物引发的分子内不对称罗赫特-柯里尔反应

Gabriela Całka-Kuc, Szymon Buda
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引用次数: 0

摘要

本文报道了使用硒酸锂进行Rauhut-Currier反应(RC)的新方法,该方法在非不对称IRC反应中提供了高达80%的产率。因此,我们的论文涉及在不对称版本中寻找一种有效的手性添加剂。考察了溶剂、添加剂、温度、时间等参数对反应的影响。在有水的情况下,非对称版本的结果明显更高,但令人惊讶的是,在不对称版本中获得了不同的观察结果。其中,叔胺手性钪配合物发挥了重要作用。在手性配合物的存在下进行的反应得到了预期的产物,产率高达60%,ee高达70%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An Asymmetric Intramolecular Rauhut-Currier Reaction Initiated by Chiral Selenolate-BINOL Complexes
This work reports the new method of Rauhut-Currier reaction (RC) with the use of lithium selenolates, which provided up to 80% yield in a non-asymmetric IRC reaction. Therefore, our paper involves the search for an efficient chiral additive in the asymmetric version. The influence of various reaction parameters, such as solvent, additives, temperature, and time, was examined. The results for the non-asymmetric version were significantly higher with the presence of water, but surprisingly different observations were obtained in the asymmetric version. Here, the chiral scandium complex with tertiary amine played an important role. The reaction carried out in the presence of chiral complexes gave the expected product with up to 60% yield and up to 70% ee.
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