Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Olga Yu. Karlutova"'
Autor:
Vladimir P. Rybalkin, Sofiya Yu. Zmeeva, Lidiya L. Popova, Irina V. Dubonosova, Olga Yu. Karlutova, Oleg P. Demidov, Alexander D. Dubonosov, Vladimir A. Bren
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 20, Iss 1, Pp 552-560 (2024)
A series of novel photo- and ionochromic N-acylated 2-(aminomethylene)benzo[b]thiophene-3(2Н)-ones with a terminal phenanthroline receptor substituent was synthesized. Upon irradiation in acetonitrile or DMSO with light of 436 nm, they underwent Z
Externí odkaz:
https://doaj.org/article/51cfabefe41c4ae08036f9f2b2518862
Autor:
Vladimir P. Rybalkin, Sofiya Yu. Zmeeva, Lidiya L. Popova, Valerii V. Tkachev, Andrey N. Utenyshev, Olga Yu. Karlutova, Alexander D. Dubonosov, Vladimir A. Bren, Sergey M. Aldoshin, Vladimir I. Minkin
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 16, Iss 1, Pp 1820-1829 (2020)
2-Benzo[b]thienyl fulgides and fulgimides containing bulky diphenylmethylene substituents were synthesized in the form of their ring-opened E- or Z-isomers. In contrast to the majority of known fulgides/fulgimides, that form colored ring-closed struc
Externí odkaz:
https://doaj.org/article/1a8887b3d4f1407db1d784ec39ecf514
Autor:
Vladimir P. Rybalkin, Sofiya Yu. Zmeeva, Lidiya L. Popova, Olga Yu. Karlutova, Alexander D. Dubonosov, Vladimir A. Bren, Vladimir I. Minkin
Publikováno v:
ARKIVOC, Vol 2019, Iss 6, Pp 15-26 (2019)
Externí odkaz:
https://doaj.org/article/920b5195e0244ecca7f8ee699310cbb9
Autor:
L. L. Popova, Vladimir I. Minkin, Vladimir A. Bren, Alexander D. Dubonosov, V. P. Rybalkin, Olga Yu. Karlutova, Sofiya Yu. Zmeeva
Publikováno v:
ARKIVOC, Vol 2019, Iss 6, Pp 15-26 (2019)
Autor:
Vladimir P. Rybalkin, Sofiya Yu. Zmeeva, Lidiya L. Popova, Gennadii S. Borodkin, Valerii V. Tkachev, Andrey N. Utenyshev, Olga Yu. Karlutova, Irina V. Dubonosova, Anatoly V. Chernyshev, Alexander D. Dubonosov, Anatoly V. Metelitsa, Vladimir A. Bren, Sergey M. Aldoshin, Vladimir I. Minkin
Publikováno v:
Journal of Photochemistry and Photobiology A: Chemistry. 427:113793
Autor:
Vitaly А. Podshibyakin, Еvgenii N. Shepelenko, Olga Yu. Karlutova, Irina V. Dubonosova, Gennadii S. Borodkin, Oksana S. Popova, Svetlana B. Zaichenko, Alexander D. Dubonosov, Vladimir A. Bren, Vladimir I. Minkin
Publikováno v:
Tetrahedron. 110:132710
Autor:
Alexander D. Dubonosov, Olga Yu. Karlutova, Еvgenii N. Shepelenko, Vladimir I. Minkin, Lyudmila G. Kuzmina, Vladimir A. Bren, Vitaly А. Podshibyakin
Publikováno v:
Journal of Molecular Structure. 1243:130758
An effective approach to the synthesis of diarylethene-amino acid hybrids DE-Gly, DE-AABA and DE-DAA (5a-d - 7-a-d) was developed via condensation of furan-2,5-dione-based diarylethenes (DE) and ethyl esters of glycine (Gly), α-aminobutyric acid (AA
Autor:
I. O. Tupaeva, Eugeny A. Gusakov, Irina V. Dubonosova, Andrey G. Starikov, Alexander D. Dubonosov, Olga Yu. Karlutova, Yury A. Sayapin, Valerii V. Tkachev, Sergey M. Aldoshin
Publikováno v:
Tetrahedron. 84:132030
Сhemosensors based on 1H-indole, 1H-benzo[e]indole, and 1H-benzo[g]indole were synthesized. According to 1H, 13C NMR, X-ray diffraction study and DFT calculations, they exist predominantly in keto form, which absorbs at 371–404 nm and exhibit a lo
Autor:
Alexander D. Dubonosov, Valerii V. Tkachev, Yurii V. Revinskii, Andrey G. Starikov, Sergey M. Aldoshin, Andrey N. Utenyshev, O. S. Popova, Vladimir I. Minkin, Olga Yu. Karlutova, Vladimir A. Bren
Publikováno v:
Journal of Molecular Structure. 1199:127013
A series of stable, potentially prototropic and ionochromic azomethine imines based on the 5-phenylpyrazolidine-3-one was synthesized and investigated. According to 1H, 13C, 15N NMR spectroscopy and X-ray diffraction data compounds containing 2,3-dih
Autor:
A. S. Cheprasov, O. G. Nikolaeva, Alexander D. Dubonosov, Igor V. Dorogan, Vladimir A. Bren, Olga Yu. Karlutova, Anatoly V. Metelitsa
Publikováno v:
Chemistry of Heterocyclic Compounds. 51:229-233
Synthesis of new asymmetric bis-spiropyrans of indoline series based on 6,8-diformyl-5,7-dihydroxy-4-methylcoumarin was realized. Depending on the nature of the substituents in positions 1 and 5 of the indoline moiety the derived compounds may exist