Addition of N-hydroxyphthalimide and atmospheric oxygen to styrenes using tert-butyl hydroperoxide as a radical initiator
- Authors: Krylov I.B.1, Budnikov A.S.1,2, Lastovko A.V.1,3, Ibatov Y.A.1,2, Nikishin G.I.1, Terent′ev A.O.1,2
- 
							Affiliations: 
							- N. D. Zelinsky Institute of Organic Chemistry of the Russian Academy of Sciences
- D. I. Mendeleev University of Chemical Technology of Russia
- M. V. Lomonosov Moscow State University
 
- Issue: Vol 68, No 7 (2019)
- Pages: 1454-1457
- Section: Brief Communications
- URL: https://journals.rcsi.science/1066-5285/article/view/243438
- DOI: https://doi.org/10.1007/s11172-019-2577-1
- ID: 243438
Cite item
Abstract
1-Aryl-1-hydroperoxy-2-imidooxyethanes are selectively formed at room temperature from styrenes, N-hydroxyphthalimide, and atmospheric oxygen with the participation of tert-butyl hydroperoxide as a radical initiator.
About the authors
I. B. Krylov
N. D. Zelinsky Institute of Organic Chemistry of the Russian Academy of Sciences
														Email: terentev@ioc.ac.ru
				                					                																			                												                	Russian Federation, 							47 Leninsky prosp., Moscow, 119991						
A. S. Budnikov
N. D. Zelinsky Institute of Organic Chemistry of the Russian Academy of Sciences; D. I. Mendeleev University of Chemical Technology of Russia
														Email: terentev@ioc.ac.ru
				                					                																			                												                	Russian Federation, 							47 Leninsky prosp., Moscow, 119991; 9 Miusskaya pl., Moscow, 125047						
A. V. Lastovko
N. D. Zelinsky Institute of Organic Chemistry of the Russian Academy of Sciences; M. V. Lomonosov Moscow State University
														Email: terentev@ioc.ac.ru
				                					                																			                												                	Russian Federation, 							47 Leninsky prosp., Moscow, 119991; 1 Leninskie Gory, Moscow, 119991						
Y. A. Ibatov
N. D. Zelinsky Institute of Organic Chemistry of the Russian Academy of Sciences; D. I. Mendeleev University of Chemical Technology of Russia
														Email: terentev@ioc.ac.ru
				                					                																			                												                	Russian Federation, 							47 Leninsky prosp., Moscow, 119991; 9 Miusskaya pl., Moscow, 125047						
G. I. Nikishin
N. D. Zelinsky Institute of Organic Chemistry of the Russian Academy of Sciences
														Email: terentev@ioc.ac.ru
				                					                																			                												                	Russian Federation, 							47 Leninsky prosp., Moscow, 119991						
A. O. Terent′ev
N. D. Zelinsky Institute of Organic Chemistry of the Russian Academy of Sciences; D. I. Mendeleev University of Chemical Technology of Russia
							Author for correspondence.
							Email: terentev@ioc.ac.ru
				                					                																			                												                	Russian Federation, 							47 Leninsky prosp., Moscow, 119991; 9 Miusskaya pl., Moscow, 125047						
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