A
A. O. Terent"ev
Researcher at Russian Academy of Sciences
Publications - 8
Citations - 63
A. O. Terent"ev is an academic researcher from Russian Academy of Sciences. The author has contributed to research in topics: tert-Butyl hydroperoxide & Catalysis. The author has an hindex of 4, co-authored 8 publications receiving 57 citations. Previous affiliations of A. O. Terent"ev include D. Mendeleev University of Chemical Technology of Russia.
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Journal ArticleDOI
Synthesis of peroxide compounds by the BF3-catalyzed reaction of acetals and enol ethers with H2O2
A. O. Terent"ev,Alexander V. Kutkin,M. M. Platonov,Ivan I. Vorontsov,M. Yu. Antipin,Yu. N. Ogibin,G. I. Nikishin +6 more
TL;DR: Aliphatic and alicyclic gem-bis-hydroperoxides and their derivatives, bis(1-hydric peroxides), dispiro-and tetraalkyl-1,2,4,5-tetroxanes were synthesized by the reaction of aliphatic alicycic acetals and enol ethers with H2O2 in the presence of BF3 in anhydrous Et2O.
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Addition of N -hydroxyphthalimide and atmospheric oxygen to styrenes using tert -butyl hydroperoxide as a radical initiator
Igor B. Krylov,Alexander S. Budnikov,Alexander S. Budnikov,A. V. Lastovko,A. V. Lastovko,Y. A. Ibatov,Y. A. Ibatov,G. I. Nikishin,A. O. Terent"ev,A. O. Terent"ev +9 more
TL;DR: In this article, 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.
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Synthesis of nine-, ten-, and fifteen-membered alkenolides by the oxidative cleavage of the bridging C = C bond in 2-oxabicycloalkenes
TL;DR: In this paper, the Cu(OAc)2-catalyzed decomposition of the resulting hydroperoxides afforded nine-, ten-, or fifteen-membered trans-alkenolides, respectively.
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Peroxidation of β-diketones and β-keto esters with tert-butyl hydroperoxide in the presence of Cu(ClO4)2/SiO2
TL;DR: In this article, β-diketones and β-keto esters with tert-butyl hydroperoxide under heterogeneous conditions using SiO2-supported copper(II) perchlorate as a catalyst give rise to α-peroxidation products in 65-82% yields.
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Electrooxidative transformation of unsubstituted and substituted nitro hydrocarbons into carbonyl compounds
TL;DR: In this article, a mixture of the corresponding aldehydes, their acetals, and methyl carboxylates were formed under similar conditions from the salts of primary nitro compounds.