Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Almira R. Miftyakhova"'
Autor:
Alisa A. Nevskaya, Lada V. Anikina, Rosa Purgatorio, Marco Catto, Orazio Nicolotti, Modesto de Candia, Leonardo Pisani, Tatiana N. Borisova, Almira R. Miftyakhova, Aleksey V. Varlamov, Elena Yu. Nevskaya, Roman S. Borisov, Leonid G. Voskressensky, Cosimo D. Altomare
Publikováno v:
Molecules, Vol 26, Iss 2, p 359 (2021)
Marine alkaloids belonging to the lamellarins family, which incorporate a 5,6-dihydro-1-phenylpyrrolo[2,1-a]isoquinoline (DHPPIQ) moiety, possess various biological activities, spanning from antiviral and antibiotic activities to cytotoxicity against
Externí odkaz:
https://doaj.org/article/18a924e640294c7d9662a70d8de2fee5
Autor:
Maria D. Matveeva, Dmitry I. Zhilyaev, Almira R. Miftyakhova, Pavel Chulkin, Patryk Janasik, Leonid G. Voskressensky, Giovanni Talarico, Ilya V. Efimov
Publikováno v:
New Journal of Chemistry. 46:5725-5729
Using 3-phenyl-5-(5-phenyl-1H-pyrrol-3-yl)-1,2,4-oxadiazole, BODIPYs with the oxadiazole groups at the 1,7-positions were prepared and their photophysical properties were characterized. The method employs 2,4-diphenyl substituted pyrrole and various
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f6e263785442ed67e1d5fe1ecb0ab1c
https://doi.org/10.1039/d1nj05317e
https://doi.org/10.1039/d1nj05317e
Autor:
Ilya V. Efimov, Almira R. Miftyakhova, Maria D. Matveeva, Dmitry I. Zhilyaev, Paweł. Czulkin, Patryk Janasik, Giovanni Talarico, Leonid G. Voskressensky
Publikováno v:
New Journal of Chemistry. 46:19291-19300
A series of new boron-dipyrromethenes bearing an aroyl functionality have been efficiently synthesized through the reaction of 2,4-disubstituted pyrroles with aromatic aldehydes followed by oxidation with DDQ and reaction with BF3OEt2. The investigat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e0889e07dfcda629a56d5315d53feea
https://doi.org/10.1039/d2nj04237a
https://doi.org/10.1039/d2nj04237a
Autor:
Maria D. Matveeva, Tatyana Yu. Zheleznova, Anastasia S. Kostyuchenko, Almira R. Miftyakhova, Dmitry I. Zhilyaev, Leonid G. Voskressensky, Giovanni Talarico, Ilya V. Efimov
Publikováno v:
ChemistrySelect. 8
A range of novel BODIPYs with the isoxazolyl groups at 1,7-positions were prepared from 3-(4-chlorophenyl)-5-(5-phenyl-1H-pyrrol-3-yl)isoxazole and their photophysical properties were characterized. The presence of the isoxazolyl groups at 1,7-positi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::573009839c79a2cb069bcc501b072d93
https://doi.org/10.1002/slct.202204465
https://doi.org/10.1002/slct.202204465
Autor:
Ilya V. Efimov, Larisa N. Kulikova, Almira R. Miftyakhova, Maria D. Matveeva, Leonid G. Voskressensky
Publikováno v:
ChemistrySelect. 6:13740-13772
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ed82d9e28358f37bec4b5763789d4092
https://doi.org/10.1002/slct.202103486
https://doi.org/10.1002/slct.202103486
Autor:
Roman A. Novikov, Alexander A. Titov, Tatiana N. Borisova, Matvey B Sidakov, Ilya V. Efimov, Almira R. Miftyakhova, Leonid G. Voskressensky, Alexey V. Varlamov
Publikováno v:
Chemistrybiodiversity. 19(1)
Synthesis of novel C3-substituted 5,6-dihydropyrrolo[2,1-a]isoquinolines via a three-component domino reaction of 1-aroyl-3,4-dihydroisoquinolines, terminal alkynes and CH-acids under microwave irradiation in dry acetonitrile is described. The method
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77cd1821519edcef724bceac9769fe42
https://pubmed.ncbi.nlm.nih.gov/34752012
https://pubmed.ncbi.nlm.nih.gov/34752012
Autor:
Almira R. Miftyakhova, Matvey B. Sidakov, Tatiana N. Borisova, Valentina V. Ilyushenkova, Artem N. Fakhrutdinov, Elena A. Sorokina, Alexey V. Varlamov, Leonid G. Voskressensky
Publikováno v:
Tetrahedron Letters. 103:153991
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5cb5e60eac24d809157c4f0989926170
https://doi.org/10.1016/j.tetlet.2022.153991
https://doi.org/10.1016/j.tetlet.2022.153991
Autor:
Orazio Nicolotti, Roman S. Borisov, Modesto de Candia, Cosimo Altomare, Elena Yu. Nevskaya, Leonardo Pisani, Aleksey V. Varlamov, Lada V. Anikina, Tatiana N. Borisova, Leonid G. Voskressensky, Marco Catto, Rosa Purgatorio, Almira R. Miftyakhova, Alisa A. Nevskaya
Publikováno v:
Molecules
Volume 26
Issue 2
Molecules, Vol 26, Iss 359, p 359 (2021)
Volume 26
Issue 2
Molecules, Vol 26, Iss 359, p 359 (2021)
Marine alkaloids belonging to the lamellarins family, which incorporate a 5,6-dihydro-1-phenylpyrrolo[2,1-a]isoquinoline (DHPPIQ) moiety, possess various biological activities, spanning from antiviral and antibiotic activities to cytotoxicity against
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1e532bcc5e1c3fc009c2749f59b3a0f
Autor:
Aleksey V. Varlamov, Tatiana N. Borisova, Leonid G. Voskressensky, Almira R. Miftyakhova, Alisa A. Nevskaya, Lada V. Anikina
Publikováno v:
Tetrahedron Letters. 87:153552
An efficient approach to the synthesis of indolizines and pyrrolo[2,1–a]isoquinolines based on a domino reaction is described. The reactivity of the derivatives and the structure-activity analysis are carried out in a number of the obtained compoun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a82ec3d980a2071c644d9587f7104af
https://doi.org/10.1016/j.tetlet.2021.153552
https://doi.org/10.1016/j.tetlet.2021.153552
Autor:
Alexander F. Smol'yakov, Dmitry I. Zhilyaev, Ilya V. Efimov, Leonid G. Voskressensky, Maria D. Matveeva, Almira R. Miftyakhova, Oleg S. Eltsov, Giovanni Talarico
Publikováno v:
Journal of Fluorine Chemistry. 249:109863
A mild, simple and efficient method for the synthesis of ortho, meta and para-fluoroaryl substituted pyrroles was discovered. It was found by NMR spectroscopy, that ortho-fluoroaryl substituted pyrroles exist in the form of inhibited conformational i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b6cf5f5162d75314c4343690d2a7a3e
https://doi.org/10.1016/j.jfluchem.2021.109863
https://doi.org/10.1016/j.jfluchem.2021.109863