Selective synthesis of cyclic triperoxides from 1,1′-dihydroperoxydi(cycloalkyl)peroxides and acetals using SnCl4
- Авторы: Radulov P.S.1,2, Belyakova Y.Y.1, Demina A.A.3, Nikishin G.I.1, Yaremenko I.A.1,2,4, Terent’ev A.O.1,2,4
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							Учреждения: 
							- N. D. Zelinsky Institute of Organic Chemistry of the Russian Academy of Sciences
- All-Russia Research Institute for Phytopathology
- M. V. Lomonosov Moscow State University
- D. I. Mendeleev University of Chemical Technology of Russia
 
- Выпуск: Том 68, № 6 (2019)
- Страницы: 1289-1292
- Раздел: Brief Communication
- URL: https://journals.rcsi.science/1066-5285/article/view/243416
- DOI: https://doi.org/10.1007/s11172-019-2555-7
- ID: 243416
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Аннотация
A method for the synthesis of 1,2,4,5,7,8-hexaoxonanes by the reaction of 1,1′-dihydroperoxydi(cycloalkyl)peroxides with acetals using SnCl4 has been developed. For the first time, it was shown that SnCl4 can serve as an effective reagent for the synthesis of cyclic organic peroxides. The proposed method allows obtaining 9-membered cyclic triperoxides selectively and in the yields of up to 90% based on the isolated product.
Об авторах
P. Radulov
N. D. Zelinsky Institute of Organic Chemistry of the Russian Academy of Sciences; All-Russia Research Institute for Phytopathology
														Email: terentev@ioc.ac.ru
				                					                																			                												                	Россия, 							47 Leninsky prosp., Moscow, 119991; 5 ul. Institut, Bolshie Vyazyomy, Odintsovo District, Moscow Region, 143050						
Yu. Belyakova
N. D. Zelinsky Institute of Organic Chemistry of the Russian Academy of Sciences
														Email: terentev@ioc.ac.ru
				                					                																			                												                	Россия, 							47 Leninsky prosp., Moscow, 119991						
A. Demina
M. V. Lomonosov Moscow State University
														Email: terentev@ioc.ac.ru
				                					                																			                												                	Россия, 							1-3 Leninskiye Gory, Moscow, 119991						
G. Nikishin
N. D. Zelinsky Institute of Organic Chemistry of the Russian Academy of Sciences
														Email: terentev@ioc.ac.ru
				                					                																			                												                	Россия, 							47 Leninsky prosp., Moscow, 119991						
I. Yaremenko
N. D. Zelinsky Institute of Organic Chemistry of the Russian Academy of Sciences; All-Russia Research Institute for Phytopathology; D. I. Mendeleev University of Chemical Technology of Russia
														Email: terentev@ioc.ac.ru
				                					                																			                												                	Россия, 							47 Leninsky prosp., Moscow, 119991; 5 ul. Institut, Bolshie Vyazyomy, Odintsovo District, Moscow Region, 143050; 9 Miusskaya pl., Moscow, 125047						
A. Terent’ev
N. D. Zelinsky Institute of Organic Chemistry of the Russian Academy of Sciences; All-Russia Research Institute for Phytopathology; D. I. Mendeleev University of Chemical Technology of Russia
							Автор, ответственный за переписку.
							Email: terentev@ioc.ac.ru
				                					                																			                												                	Россия, 							47 Leninsky prosp., Moscow, 119991; 5 ul. Institut, Bolshie Vyazyomy, Odintsovo District, Moscow Region, 143050; 9 Miusskaya pl., Moscow, 125047						
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