Synthesis of spiro(pyrrol-2,5'-pyrrolo[2,3-d]pyrimidine)2',4',5,6'-tetraones by the reaction of pyrrolo[2,1-c][1,4]oxazinetriones with 6-aminopyrimidine-2,4-diones
- 作者: Tretyakov N.A1, Dmitriev M.V1, Maslivets A.N1
 - 
							隶属关系: 
							
- Perm State University
 
 - 期: 卷 59, 编号 2 (2023)
 - 页面: 180-186
 - 栏目: Articles
 - URL: https://clinpractice.ru/0514-7492/article/view/666384
 - DOI: https://doi.org/10.31857/S0514749223020039
 - EDN: https://elibrary.ru/QIZBLZ
 - ID: 666384
 
如何引用文章
详细
8-Aroyl-3,4-dihydro-1 H -pyrrolo[2,1- c ][1,4]oxazine-1,6,7-triones react with 6-aminopyrimidine-2,4(1 H ,3 H )diones to form 3-aroyl-4-hydroxy-1-(2-hydroxyalkyl)spiro(pyrrole-2,5'-pyrrolo[2,3- d ]pyrimidine)2',4',5,6'(1 H ,1' H ,3' H ,7' H )-tetraones, the structure of which was confirmed by X-ray diffraction analysis.
			                作者简介
N. Tretyakov
Perm State University
														Email: koh2@psu.ru
				                					                																			                												                														
M. Dmitriev
Perm State University
														Email: koh2@psu.ru
				                					                																			                												                														
A. Maslivets
Perm State University
														Email: koh2@psu.ru
				                					                																			                												                														
参考
- Денисламова Е.С., Банникова Ю.Н., Масливец А.Н. ЖОрХ. 2009, 45, 1272-1273.
 - Denislamova E.S., Bannikova Yu.N., Maslivets A.N. Russ. J. Org. Chem. 2009, 45, 1264-1265. doi: 10.1134/S1070428009080302
 - Денисламова Е.С., Бубнов Н.В., Масливец А.Н. ЖОрХ. 2011, 47, 915-918.
 - Denislamova E.S., Bubnov N.V., Maslivets A.N. Russ. J. Org. Chem. 2011, 47, 933-936. doi: 10.1134/S1070428011060170
 - Силайчев П.С., Масливец А.Н. ЖОрХ. 2013, 49, 958-959.
 - Silaichev P.S., Maslivets A.N. Russ. J. Org. Chem. 2013, 49, 945-946. doi: 10.1134/S1070428013060298
 - ElKalyoubi S., Fayed E. J. Chem. Res. 2016, 40, 771-776. doi: 10.3184/174751916X14798125870610
 - Mohammadizadeh M.R., Azizian J., Teimouri F., Mohammadi A.A., Karimi A.R., Tamari E. Can. J. Chem. 2008, 86, 925-929. doi: 10.1139/V08-117
 - Dabiri M., Azimi S.C., Khavasi H.R., Bazgir A. Tetrahedron. 2008, 64, 7307-7311. doi: 10.1016/j.tet.2008.05.063
 - Ghahremanzadeh R., Azimi S.C., Gholami N., Bazgir A. Chem. Pharm. Bull. 2008, 56, 1617-1620. doi: 10.1248/cpb.56.1617
 - Baradarani M.M., Farshi H., Khodaie M., Fazlelahi H.Z., Rashidi A., Joulec J.A. J. Heterocycl. Chem. 2017, 55, 91-96. doi: 10.1002/jhet.3008
 - Spek A.L. Acta Crystallogr., Sect. C. 2015, 71, 9-18. doi: 10.1107/S2053229614024929
 - CrysAlisPro, Agilent Technologies, Version 1.171.37.33 (release 27-03-2014 CrysAlis171.NET).
 - Sheldrick G.M. Acta Crystallogr., Sect. A. 2008, 64, 112-122. doi: 10.1107/S0108767307043930
 - Sheldrick G.M. Acta Crystallogr., Sect. A. 2015, 71, 3-8. doi: 10.1107/S2053273314026370
 - Sheldrick G.M. Acta Crystallogr., Sect. C. 2015, 71, 3-8. doi: 10.1107/S2053229614024218
 - Dolomanov O.V., Bourhis L.J., Gildea R.J., Howard J.A.K., Puschmann H. J. Appl. Crystallogr. 2009, 42, 339. doi: 10.1107/S0021889808042726
 - Третьяков Н.А., Шаврина Т.В., Масливец А.Н. ЖОрХ. 2019, 55, 791-793.
 - Tretyakov N.A., Shavrina T.V., Maslivets A.N. Russ. J. Org. Chem. 2019, 55, 719-720. doi: 10.1134/S1070428019050221
 
补充文件
				
			
						
						
						
						
					


