Synthesis and application of N-hydroxy(tetrahydrofuran-2-yl)amines
- 作者: Vasilenko D.А.1, Averina E.B.1,2,3, Sedenkova К.N.1,2,3, Kuznetsova Т.S.1, Zefirov N.S.1
- 
							隶属关系: 
							- Department of Chemistry, M. V. Lomonosov Moscow State University
- N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
- Institute of Physiologically Active Compounds, Russian Academy of Sciences
 
- 期: 卷 66, 编号 11 (2017)
- 页面: 1963-1981
- 栏目: Review
- URL: https://journals.rcsi.science/1066-5285/article/view/241496
- DOI: https://doi.org/10.1007/s11172-017-1972-8
- ID: 241496
如何引用文章
详细
Data on synthesis, reactivity and bioactivity of N-hydroxy(tetrahydrofuran-2-yl)amines were discussed in the present review. General approaches to chiral N-glycosylhydroxylamines based on reactions of hydroxylamine with cyclic five-membered hemiacetals or dihydrofurans as well as reactions of tetrahydrofuran-containing nitrones with nucleophiles were systematized. The application of N-hydroxy(tetrahydrofuran-2-yl)amines in the synthesis of chiral heterocycles, aminophosphonic acids, N-hydroxypropargylamines, as well as natural compounds (for example, sieboldin A), pharmaceuticals (Zileuton) and their analogs was demonstrated. It was found that depending on substituents, N-hydroxy(tetrahydrofuran-2-yl)-amines can act as lipoxygenase inhibitors, and show antioxidant, antitumor, antibacterial, and other types of activities.
作者简介
D. Vasilenko
Department of Chemistry, M. V. Lomonosov Moscow State University
														Email: elaver@org.chem.msu.ru
				                					                																			                												                	俄罗斯联邦, 							1-3 Leninskie Gory, Moscow, 119991						
E. Averina
Department of Chemistry, M. V. Lomonosov Moscow State University; N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences; Institute of Physiologically Active Compounds, Russian Academy of Sciences
							编辑信件的主要联系方式.
							Email: elaver@org.chem.msu.ru
				                					                																			                												                	俄罗斯联邦, 							1-3 Leninskie Gory, Moscow, 119991; 47 Leninsky Prosp., Moscow, 119991; 1 Severnyi proezd, 142432 Chernogolovka, Moscow Region						
К. Sedenkova
Department of Chemistry, M. V. Lomonosov Moscow State University; N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences; Institute of Physiologically Active Compounds, Russian Academy of Sciences
														Email: elaver@org.chem.msu.ru
				                					                																			                												                	俄罗斯联邦, 							1-3 Leninskie Gory, Moscow, 119991; 47 Leninsky Prosp., Moscow, 119991; 1 Severnyi proezd, 142432 Chernogolovka, Moscow Region						
Т. Kuznetsova
Department of Chemistry, M. V. Lomonosov Moscow State University
														Email: elaver@org.chem.msu.ru
				                					                																			                												                	俄罗斯联邦, 							1-3 Leninskie Gory, Moscow, 119991						
N. Zefirov
Department of Chemistry, M. V. Lomonosov Moscow State University
														Email: elaver@org.chem.msu.ru
				                					                																			                												                	俄罗斯联邦, 							1-3 Leninskie Gory, Moscow, 119991						
补充文件
 
				
			 
						 
						 
					 
						 
						 
				 
  
  
  
  
  电邮这篇文章
			电邮这篇文章  开放存取
		                                开放存取 ##reader.subscriptionAccessGranted##
						##reader.subscriptionAccessGranted## 订阅存取
		                                		                                        订阅存取
		                                					