Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Nataliya N. Mochulskaya"'
Autor:
Nataliya N. Mochulskaya, Svetlana K. Kotovskaya, Ilya I. Butorin, Mikhail V. Varaksin, Valery N. Charushin, Vladimir L. Rusinov, Yana L. Esaulkova, Alexander V. Slita, Polina A. Ilyina, Vladimir V. Zarubaev
Publikováno v:
Chemistry, Vol 5, Iss 4, Pp 2657-2676 (2023)
A series of 2,4-disubstituted pyrrolo[2,1-f][1,2,4]triazines containing both aryl and thienyl substituents were synthesized by exploiting the 1,3-cycloaddition reaction of N(1)-ethyl-1,2,4-triazinium tetrafluoroborates with dimethyl acetylenedicarbox
Externí odkaz:
https://doaj.org/article/bf9d38349d5c4072b8641c1f4806d93c
Autor:
Igor A. Khalymbadzha, Ramil F. Fatykhov, Ilya I. Butorin, Ainur D. Sharapov, Anastasia P. Potapova, Nibin Joy Muthipeedika, Grigory V. Zyryanov, Vsevolod V. Melekhin, Maria D. Tokhtueva, Sergey L. Deev, Marina K. Kukhanova, Nataliya N. Mochulskaya, Mikhail V. Tsurkan
Publikováno v:
Biomimetics, Vol 9, Iss 1, p 44 (2024)
We have designed and synthesized a series of bioinspired pyrano[2,3-f]coumarin-based Calanolide A analogs with anti-HIV activity. The design of these new calanolide analogs involved incorporating nitrogen heterocycles or aromatic groups in lieu of ri
Externí odkaz:
https://doaj.org/article/bb4f6881cd7241e0897dfbe5f9b17b6d
Publikováno v:
Chimica Techno Acta, Vol 7, Iss 3, Pp 96-103 (2020)
A series of 2-hetaryl- and 2-(hetaryl)ylidene substituted 5-fluoro-8-nitro-1,3-benzothiazin-4-ones was synthesized by interaction of 2,6-difluoro-3-nitrobenzoylisothiocyanate with C-nucleophiles. Cyclocondensation of polyfluorobenzoylchlorides with a
Externí odkaz:
https://doaj.org/article/a2182820d5e7436b95e934b59c909682
Autor:
Ramil F. Fatykhov, Igor A. Khalymbadzha, Ainur D. Sharapov, Anastasia P. Potapova, Nataliya N. Mochulskaya, Anton N. Tsmokalyuk, Alexandra V. Ivoilova, Polina N. Mozharovskaia, Sougata Santra, Oleg N. Chupakhin
Publikováno v:
Molecules, Vol 27, Iss 20, p 7105 (2022)
A different type of MnO2-induced oxidative cyclization of dihydrotriazines has been developed. These dihydrotriazines are considered as a “formal” Schiff’s base. This method provided easy access to naphthofuro-fused triazine via the C-C/C-O oxi
Externí odkaz:
https://doaj.org/article/b0c54c8bb6d740f68cec2dade8780d5d
Autor:
Chupakhin, Ramil F. Fatykhov, Igor A. Khalymbadzha, Ainur D. Sharapov, Anastasia P. Potapova, Nataliya N. Mochulskaya, Anton N. Tsmokalyuk, Alexandra V. Ivoilova, Polina N. Mozharovskaia, Sougata Santra, Oleg N.
Publikováno v:
Molecules; Volume 27; Issue 20; Pages: 7105
A different type of MnO2-induced oxidative cyclization of dihydrotriazines has been developed. These dihydrotriazines are considered as a “formal” Schiff’s base. This method provided easy access to naphthofuro-fused triazine via the C-C/C-O oxi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::9a5c5c776e3cf117fda3759e0b48f3c0
Autor:
Ramil F, Fatykhov, Igor A, Khalymbadzha, Ainur D, Sharapov, Anastasia P, Potapova, Nataliya N, Mochulskaya, Anton N, Tsmokalyuk, Alexandra V, Ivoilova, Polina N, Mozharovskaia, Sougata, Santra, Oleg N, Chupakhin
Publikováno v:
Molecules (Basel, Switzerland). 27(20)
A different type of MnO
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b7ffd592be82876068d11579db94cedc
https://pubmed.ncbi.nlm.nih.gov/36296698
https://pubmed.ncbi.nlm.nih.gov/36296698
Autor:
Marina A. Ezhikova, Valery N. Charushin, Marionella A. Kravchenko, Emiliya V. Nosova, Svetlana K. Kotovskaya, Mikhail I. Kodess, Fedor V. Antipin, Nataliya N. Mochulskaya
Publikováno v:
Journal of Fluorine Chemistry. 208:15-23
An efficient method for incorporation of the cyanomethyl fragment into the benzene ring of bi- and tricyclic fluoroquinolones through the nucleophilic substitution of a fluorine atom with carbanions derived from CH-active cyanoacetates, followed by a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0998f45e07e4119e028e0d469b4da515
https://doi.org/10.1016/j.jfluchem.2018.01.007
https://doi.org/10.1016/j.jfluchem.2018.01.007
Autor:
E. A. Savateeva, Oleg N. Chupakhin, V. V. Emel’yanov, N. E. Maksimova, Nataliya N. Mochulskaya, Tatyana A. Tseitler, Valery A. Chereshnev, L. P. Sidorova
Publikováno v:
Pharmaceutical Chemistry Journal. 51:9-12
Cyclocondensation of α-halogenacetophenones with an original 4-morpholine thiosemicarbazide was used to synthesize a group of new Captions: of the 1,3,4-thiadiazine group, containing a thiomorpholine fragment at position 2 of the thiadiazine ring. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f4a955cdf56dfa46348e6564e32d9d9d
https://doi.org/10.1007/s11094-017-1547-x
https://doi.org/10.1007/s11094-017-1547-x
Publikováno v:
Mendeleev Communications. 26:375-377
Reaction of 3-aryl-1,2,4-triazines with S,N-dinucleophilic N-(het)arylthioureas in acetic anhydride at room temperature affords the cyclization products, tetrahydrothiazolo[4,5-e]-[1,2,4]triazines in good yields. The structure of the heterocyclic sys
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a63714e5b464a5aa28c95794a2e69cbb
https://doi.org/10.1016/j.mencom.2016.09.002
https://doi.org/10.1016/j.mencom.2016.09.002
Autor:
Valery N. Charushin, Oleg N. Chupakhin, Antatoly A. Andreiko, Mikhail I. Kodess, Vera I. Filyakova, Nataliya N. Mochulskaya
Publikováno v:
Tetrahedron Letters. 44:2421-2424
5,6-Unsubstituted-3-aryl-1,2,4-triazines were found to react with aminovinyl ketones and aminovinyl esters in acetic anhydride to form derivatives of 3a,4,7,7a-tetrahydro-1H-pyrrolo[3,2-e]1,2,4-triazines in good yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a27fe0d6f12f3cf621d7ba3f7c2164f
https://doi.org/10.1016/s0040-4039(03)00060-1
https://doi.org/10.1016/s0040-4039(03)00060-1