Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Nikolai v. Lysenko"'
Publikováno v:
2019 IEEE Conference of Russian Young Researchers in Electrical and Electronic Engineering (EIConRus).
This article shows the possibility of detection of the hidden information in images. This is the approach to steganalysis than the basic data about the image and the information about the hiding method of the information are unknown. The architecture
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e1f98722cd56a528bcf9660f4abb77ce
https://doi.org/10.1109/eiconrus.2019.8656886
https://doi.org/10.1109/eiconrus.2019.8656886
Autor:
Dmitriy M. Volochnyuk, Yurii V. Svyaschenko, Nikolai v. Lysenko, Andrei A. Tolmachev, Alexandr M. Pinchuk, A. N. Kostyuk
Publikováno v:
Tetrahedron Letters. 44:6487-6491
The reaction of ‘push–pull’ enamines—derivatives of β-aminocrotonic acid with diphenylchlorophosphine has been investigated. Structural sensitivity of the reaction was found and is discussed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ab6f2ebc8a1e7ee4e86f0310637c4a1
https://doi.org/10.1016/s0040-4039(03)01546-6
https://doi.org/10.1016/s0040-4039(03)01546-6
Autor:
Aleksandr M. Pinchuk, Anatoly P. Marchenko, Nikolai v. Lysenko, Aleksandr N. Kostyuk, Andrei A. Tolmachev, Georgy N. Koidan
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 139:209-229
The phosphorylation reaction of 5–arylmethylidene–1–morpholinocyclopentenes with various phosphorus (III) and (V) halides was studied. It was shown that the enamines react with phosphorus (III) halides giving stable halo– and dihalophosphines
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8a9034602565b04c012cad033cd84216
https://doi.org/10.1080/10426509808035689
https://doi.org/10.1080/10426509808035689
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 147:485-485
Introduction of benzylidene group at α-position of enamines derived from cyclic ketones substantially increases strength of C-P bond thus permitting further syntheses without splitting of the C-P bond. A wide set of phosphorylated derivatives of typ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::602494183ed77b5c0037790967fb27a3
https://doi.org/10.1080/10426509908053722
https://doi.org/10.1080/10426509908053722