Recent advances in the synthesis of highly substituted imidazolidines

被引:0
作者
Olyaei, Abolfazl [1 ]
Sadeghpour, Mahdieh [2 ]
机构
[1] Imam Khomeini Int Univ, Fac Sci, Dept Chem, Qazvin, Iran
[2] Islamic Azad Univ, Dept Chem, Qazvin Branch, Qazvin, Iran
关键词
POT STEREOSELECTIVE-SYNTHESIS; MANNICH-TYPE REACTION; SCHIFF-BASE LIGAND; AZOMETHINE YLIDES; 3+2 CYCLOADDITION; BIOLOGICAL EVALUATION; EFFICIENT SYNTHESIS; ENANTIOSELECTIVE SYNTHESIS; 1,3-DIPOLAR CYCLOADDITION; ASYMMETRIC-SYNTHESIS;
D O I
10.1039/d4ra06010e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Imidazolidine is a saturated heterocycle with a cyclic aminal core that can be found in natural products and biologically active molecules. Additionally, these heterocyclic compounds have been utilized as chiral ligands, N-heterocyclic carbene precursors, and catalysts in organic synthesis. This review is an attempt to compile the literature of various synthetic procedures of highly substituted imidazolidines, chiral imidazolidines with high diastereoselectivities and enantioselectivities, bis-imidazolidines, and spiro-imidazolidines, as well as their pharmacological properties during the period from 1949 to 2023. In this highlight, recent advances in the synthesis of highly substituted imidazolidines, chiral imidazolidines with high diastereoselectivities and enantioselectivities, bis-imidazolidines, and spiro-imidazolidines are presented.
引用
收藏
页码:30758 / 30806
页数:49
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