Synthesis and transformations of O-propargyl analogues of fusidic acid
- 作者: Salimova E.V.1, Golovnina D.A.1, Parfenova L.V.1
- 
							隶属关系: 
							- Ufa Federal Research Center, Russian Academy of Sciences
 
- 期: 卷 61, 编号 3 (2025)
- 页面: 285-292
- 栏目: ЭКСПЕРИМЕНТАЛЬНЫЕ СТАТЬИ
- URL: https://rjeid.com/0514-7492/article/view/687806
- DOI: https://doi.org/10.31857/S0514749225030084
- EDN: https://elibrary.ru/EUCMMT
- ID: 687806
如何引用文章
详细
In continuation of the studies on synthetic modifications of fusidane triterpenoids, an O-propargyl fragment was introduced at the C3 atom of the fusidic acid methyl ester molecule and chemical transformations of the triple bond were carried out through reactions catalyzed by copper(I) salts to obtain an aminomethylene analogue, 1,2,3-triazole, and an aryl-substituted acetylene derivative.
全文:
 
												
	                        作者简介
E. Salimova
Ufa Federal Research Center, Russian Academy of Sciences
							编辑信件的主要联系方式.
							Email: salimovaev@mail.ru
				                	ORCID iD: 0000-0002-4328-5080
				                																			                								
Institute of Petrochemistry and Catalysis
俄罗斯联邦, prosp. Oktyabrya, 141, Ufa, 450075D. Golovnina
Ufa Federal Research Center, Russian Academy of Sciences
														Email: salimovaev@mail.ru
				                					                																			                								
Institute of Petrochemistry and Catalysis
俄罗斯联邦, prosp. Oktyabrya, 141, Ufa, 450075L. Parfenova
Ufa Federal Research Center, Russian Academy of Sciences
														Email: salimovaev@mail.ru
				                	ORCID iD: 0000-0003-2816-2178
				                																			                								
Institute of Petrochemistry and Catalysis
俄罗斯联邦, prosp. Oktyabrya, 141, Ufa, 450075参考
- Hosseininezhada S., Ramazani A. RSC Adv. 2024, 14, 278–352. doi: 10.1039/d3ra07670a
- Talele T.T. J. Med. Chem. 2020, 63, 5625−5663. doi: 10.1021/acs.jmedchem.9b01617
- Costa B., Vale N. Biomolecules. 2023, 13, 88–98. doi: 10.3390/biom13010088
- Monjur Al Hossain A.S.M., Sil B.C., Iliopoulos F., Lever R., Hadgraft J., Lane M.E. Pharmaceutics. 2019, 11, 548–561. doi: 10.3390/pharmaceutics11100548
- Vollmar B.S., Frantz C., Schutten M.M., Zhong F., Rosario G., Go M.A.T., Yu S.F., Leipold D.D., Kamath A.V., Ng C., Xu K., Cruz-Chuh J., Kozak K.R., Chen J., Xu Z., Wai J., Adhikari P., Erickson H.K., Dragovich P.S., Polson A.G., Pillow T.H. Mol. Cancer. Ther. 2021, 20, 1112–1120. doi: 10.1158/1535-7163.MCT-20-0035
- Hansen S.V., Christiansen E., Urban C., Hudson B.D., Stocker C.J., Due-Hansen M.E., Wargent E.T., Shimpukade B., Almeida R., Ejsing C.S., Cawthorne M.A., Kassack M.U., Milligan G., Ulven T. J. Med. Chem. 2016, 59, 2841−2846. doi: 10.1021/acs.jmedchem.5b01962
- Yang F., Snyder L.B., Balakrishnan A., Brown J.M., Sivarao D.V., Easton A., Fernandes A., Gulianello M., Hanumegowda U.M., Huang H., Huang Y., Jones K.M., Li Y.W., Matchett M., Mattson G., Miller R., Santone K.S., Senapati A., Shields E.E., Simutis F.J., Westphal R., Whiterock V.J., Bronson J.J., Macor J.E., Degnan A.P. ACS Med. Chem. Lett. 2016, 7, 289−293. doi: 10.1021/acsmedchemlett.5b00450
- Ramani A., Desai B., Patel M., Naveen T. Asian J. Org. Chem. 2022, 11, e202200047. doi: 10.1002/ajoc.202200047
- Kuklev D.V., Domb A.J., Dembitsky V.M. Phytomedicine. 2013, 20, 1145–1159. doi: 10.1016/j.phymed.2013.06.009
- Ольшанова А.С., Ямансаров Э.Ю., Селезнев Е.И., Ковалев С.В., Лопухов А.В., Скворцов Д.А., Евтеев С.А., Клячко Н.Л., Белоглазкина Е.К., Иваненков Я.А., Мажуга А.Г. Изв. АН. Сер. Хим. 2020, 69, 158–163. [Olshanova A.S., Yamansarov E.Yu., Seleznev E.I., Kovalev S.V, Lopuhov A.V., Skvortsov D.A., Evteev S.A., Klyachko N.L., Beloglazkina E.K., Ivanenkov Ya.A., Majouga A.G. Russ. Chem. Bull. 2020, 69, 158–163]. doi: 10.1007/s11172-020-2737-3
- Grymel M., Pastuch-Gawołek G., Lalik A., Zawojak M., Boczek S., Krawczyk M., Erfurt K. Molecules. 2020, 25, 6019–6043. doi: 10.3390/molecules25246019
- Khusnutdinova E.F., Petrova A.V., Kazakova O.B. J. Antibiot. 2024, 77, 50–56. doi: 10.1038/s41429-023-00672-5
- Petrova A.V., Kazakova O.B., Nazarov I.S., Csuk R., Heise N.V. Chem. Biodivers. 2023, 20, e202300185. doi: 10.1002/cbdv.202300185
- Grzes P.A., Sawicka A., Niemirowicz-Laskowska K., Wielgat P., Sawicka D., Car H., Jastrzebska I. J. Steroid Biochem. Mol. Biol. 2023, 227, 106232–106239. doi: 10.1016/j.jsbmb.2022.106232
- Zhao M., Gödecke T., Gunn J., Duan J.A., Che C.T. Molecules. 2013, 18, 4054–4080. doi: 10.3390/molecules18044054
- Godtfredsen W.O., Jahnsen S., Lorck H., Roholt K., Tybring L. Nature. 1962, 193, 987. doi: 10.1038/193987a0
- Tu B., Cao N., Zhang B., Zheng W., Li J., Tang X., Su K., Li J., Zhang Z., Yan Z., Li D., Zheng X., Zhang K., Hong W.D., Wu P. Antibiotics. 2022, 11, 1026–1055. doi: 10.3390/antibiotics11081026
- Salimova E.V., Parfenova L.V., Ishmetova D.V., Zainullina L.F., Vakhitova Y.V., Nat. Prod. Res. 2023, 37, 3956–3963. doi: 10.1080/14786419.2022.2163483
- Салимова Е.В., Парфенова Л.В. Изв. АН. Сер. Хим. 2024, 73, 2309–2315. [Salimova E.V., Parfenova L.V. Russ. Chem. Bull. 2024, 73, 2309–2315.] doi: 10.1007/s11172-024-4354-z
- Williamson A. J. Chem. Soc. 1852, 4, 229–239. doi: 10.1039/QJ8520400229
- Салимова Е.В., Мамаев А.Г., Третьякова Е.В., Куковинец О.С., Мавзютов А.Р., Швец К.Ю., Парфенова Л.В. ЖOрХ. 2018, 54, 1395–1402. [Salimova E.V., Mamaev A.G., Tret’yakova E.V., Kukovinets O.S., Mavzyutov A.R., Shvets K.Yu., Parfenova L.V. Russ. J. Org. Chem. 2018, 54, 1411–1418.] doi: 10.1134/S1070428018090245
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##


