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An Overview of the One-pot Synthesis of Imidazolines
Current Organic Chemistry ( IF 2.6 ) Pub Date : 2020-09-30 , DOI: 10.2174/1385272824999201001153735
Thaipparambil Aneeja 1 , Sankaran Radhika 1 , Mohan Neetha 1 , Gopinathan Anilkumar 1
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One-pot syntheses are a simple, efficient and easy methodology, which are widely used for the synthesis of organic compounds. Imidazoline is a valuable heterocyclic moiety used as a synthetic intermediate, chiral auxiliary, chiral catalyst and a ligand for asymmetric catalysis. Imidazole is a fundamental unit of biomolecules that can be easily prepared from imidazolines. The one-pot method is an impressive approach to synthesize organic compounds as it minimizes the reaction time, separation procedures, and ecological impact. Many significant one-pot methods such as N-bromosuccinimide mediated reaction, ring-opening of tetrahydrofuran, triflic anhydrate mediated reaction, etc. were reported for imidazoline synthesis. This review describes an overview of the one-pot synthesis of imidazolines and covers literature up to 2020.



中文翻译:

一锅法合成咪唑啉的概述

一锅法合成是一种简单,高效且简便的方法,已广泛用于有机化合物的合成。咪唑啉是有价值的杂环部分,用作合成中间体,手性助剂,手性催化剂和不对称催化的配体。咪唑是可以从咪唑啉轻松制备的生物分子的基本单元。一锅法是一种令人印象深刻的合成有机化合物的方法,因为它使反应时间,分离步骤和生态影响最小化。据报道,许多重要的一锅法,如N-溴琥珀酰亚胺介导的反应,四氢呋喃的开环,无水三氟甲磺酸介导的反应等,都用于咪唑啉的合成。这篇综述描述了咪唑啉的一锅法合成概述,并涵盖了2020年以前的文献。

更新日期:2020-12-02
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