Facile synthesis of pyrrolo[2,1-a]isoquinolines by domino reaction of 1-aroyl-3,4-dihydroisoquinolines with conjugated ketones, nitroalkenes and nitriles.

Autor: Astakhov GS; Department of Organic Chemistry, Peoples' Friendship, University of Russia (RUDN University), Miklukho-Maklaya st 6, Moscow, Russia, 117198.; Laboratory of Metal Hydrides (MHLab), A. N. Nesmeyanov Institute of Organoelement Compounds (INEOS), Russian Academy of Sciences, Vavilov St. 28, GSP-1, B-334, Moscow, Russia, 119991., Shigaev RR; Department of Organic Chemistry, Peoples' Friendship, University of Russia (RUDN University), Miklukho-Maklaya st 6, Moscow, Russia, 117198., Borisova TN; Department of Organic Chemistry, Peoples' Friendship, University of Russia (RUDN University), Miklukho-Maklaya st 6, Moscow, Russia, 117198., Ershova AA; Department of Organic Chemistry, Peoples' Friendship, University of Russia (RUDN University), Miklukho-Maklaya st 6, Moscow, Russia, 117198., Titov AA; Department of Organic Chemistry, Peoples' Friendship, University of Russia (RUDN University), Miklukho-Maklaya st 6, Moscow, Russia, 117198., Varlamov AV; Department of Organic Chemistry, Peoples' Friendship, University of Russia (RUDN University), Miklukho-Maklaya st 6, Moscow, Russia, 117198., Voskressensky LG; Department of Organic Chemistry, Peoples' Friendship, University of Russia (RUDN University), Miklukho-Maklaya st 6, Moscow, Russia, 117198., Matveeva MD; Department of Organic Chemistry, Peoples' Friendship, University of Russia (RUDN University), Miklukho-Maklaya st 6, Moscow, Russia, 117198. m.d.matveeva@gmail.com.

Publikováno v: Molecular diversity [Mol Divers] 2021 Nov; Vol. 25 (4), pp. 2441-2446. Date of Electronic Publication: 2020 Oct 10.

New suitable deprotonating matrices for the analysis of carboxylic acids and some acidic compounds by matrix-assisted laser desorption/ionization mass spectrometry in negative ion mode.

Autor: Krivosheina MS; A.V. Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences, Leninsky pr. 29, Moscow, 119991, Russian Federation., Borisov RS; A.V. Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences, Leninsky pr. 29, Moscow, 119991, Russian Federation.; People's Friendship University of Russia, ul. Miklukho-Maklay 6, Moscow, 117198, Russian Federation., Zhilyaev DI; A.V. Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences, Leninsky pr. 29, Moscow, 119991, Russian Federation.; People's Friendship University of Russia, ul. Miklukho-Maklay 6, Moscow, 117198, Russian Federation., Matveeva MD; A.V. Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences, Leninsky pr. 29, Moscow, 119991, Russian Federation., Zaikin VG; A.V. Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences, Leninsky pr. 29, Moscow, 119991, Russian Federation.

Publikováno v: Rapid communications in mass spectrometry : RCM [Rapid Commun Mass Spectrom] 2021 Jan 15; Vol. 35 (1), pp. e8954.

A New Class of 1-Aryl-5,6-dihydropyrrolo[2,1-a]isoquinoline Derivatives as Reversers of P-Glycoprotein-Mediated Multidrug Resistance in Tumor Cells.

Autor: Nevskaya AA; Organic Chemistry Department, Peoples' Friendship University of Russia, 6 Miklukho-Maklaya St., Moscow, 117198, Russia., Matveeva MD; Organic Chemistry Department, Peoples' Friendship University of Russia, 6 Miklukho-Maklaya St., Moscow, 117198, Russia., Borisova TN; Organic Chemistry Department, Peoples' Friendship University of Russia, 6 Miklukho-Maklaya St., Moscow, 117198, Russia., Niso M; Department of Pharmacy-Drug Sciences, University of Bari Aldo Moro, Via E. Orabona 4, 70125, Bari, Italy., Colabufo NA; Department of Pharmacy-Drug Sciences, University of Bari Aldo Moro, Via E. Orabona 4, 70125, Bari, Italy., Boccarelli A; Department of Biomedical Sciences and Human Oncology, University of Bari Aldo Moro, Piazza Giulio Cesare 11, 70124, Bari, Italy., Purgatorio R; Department of Pharmacy-Drug Sciences, University of Bari Aldo Moro, Via E. Orabona 4, 70125, Bari, Italy., de Candia M; Department of Pharmacy-Drug Sciences, University of Bari Aldo Moro, Via E. Orabona 4, 70125, Bari, Italy., Cellamare S; Department of Pharmacy-Drug Sciences, University of Bari Aldo Moro, Via E. Orabona 4, 70125, Bari, Italy., Voskressensky LG; Organic Chemistry Department, Peoples' Friendship University of Russia, 6 Miklukho-Maklaya St., Moscow, 117198, Russia., Altomare CD; Department of Pharmacy-Drug Sciences, University of Bari Aldo Moro, Via E. Orabona 4, 70125, Bari, Italy.

Publikováno v: ChemMedChem [ChemMedChem] 2018 Aug 10; Vol. 13 (15), pp. 1588-1596. Date of Electronic Publication: 2018 Jul 04.

Development of benzimidazole derivatives as efficient matrices for the analysis of acidic small-molecule compounds using matrix-assisted laser desorption/ionisation time-of-flight mass spectrometry in negative ion mode.

Autor: Cen X; School of Chemistry, Sun Yat-sen University, Guangzhou, China., Fang Y; School of Chemistry, Sun Yat-sen University, Guangzhou, China., Chen Z; Instrumental Analysis & Research Center, Sun Yat-sen University, Guangzhou, China., Zhu X; Instrumental Analysis & Research Center, Sun Yat-sen University, Guangzhou, China.

Publikováno v: Rapid communications in mass spectrometry : RCM [Rapid Commun Mass Spectrom] 2024 Jul 15; Vol. 38 (13), pp. e9751.

[Studies of fermentation activity of aerobic variants of Bac. perfringens type B obtained under the influence of roentgen rays].

Autor: PASICHNYK AM, MATVEEVA MD

Publikováno v: Mikrobiolohichnyi zhurnal [Mikrobiol Zh] 1960; Vol. 22(5), pp. 52-5.