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醛、酰肼和炔烃的催化不对称三组分 1,3-偶极环加成反应。

Catalytic asymmetric three-component 1,3-dipolar cycloaddition of aldehydes, hydrazides, and alkynes.

机构信息

Department of Chemistry, Graduate School of Science, Kyoto University, Sakyo, Kyoto 606-8502, Japan.

出版信息

J Am Chem Soc. 2013 Aug 7;135(31):11473-6. doi: 10.1021/ja405444c. Epub 2013 Jul 25.

Abstract

Catalytic asymmetric 1,3-dipolar cycloadditions offer expeditious ways to afford synthetically important chiral heterocycles. Although a variety of 1,3-dipoles can be employed in this context, the use of acyclic azomethine imines as a facile means to give chiral pyrazolines and pyrazolidines remains completely unexplored. We report herein the first catalytic asymmetric 1,3-dipolar cycloaddition of terminal alkynes with acyclic azomethine imines generated in situ from the corresponding aldehydes and hydrazides, which was realized using Cu(I)/pybox and axially chiral dicarboxylic acid cocatalysts.

摘要

催化不对称 1,3-偶极环加成反应为合成重要的手性杂环提供了快速的方法。尽管在此背景下可以使用各种 1,3-偶极子,但将无环亚甲胺亚胺作为一种简便的方法来提供手性吡唑啉和吡唑烷的用途仍完全未被探索。我们在此报告了首例使用 Cu(I)/pybox 和轴向手性二羧酸共催化剂,通过末端炔烃与无环亚甲胺亚胺的催化不对称 1,3-偶极环加成反应,其中无环亚甲胺亚胺是由相应的醛和酰肼原位生成的。

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