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Airat M. Gimazetdinov

Observed names: A. M. Gimazetdinov, A. M. Gizametdinov, A.M. Gimazetdinov, Airat M. Gimazetdinov, Gimazetdinov, A.M., А. М. ГИМАЗЕТДИНОВ, А.М. Гимазетдинов, Айрат Гимазетдинов
ORCID: 0000-0002-8539-3442
Observed ORCID: 0000-0002-8539-3442
OpenAlex ID: A5010247008
Cross-Conjugated Cyclopentenone Prostaglandins. Recent Advances
2018 · V. V. Loza, A. M. Gimazetdinov, et al. · Russian Journal of Organic Chemistry · 20
A simple and efficient synthesis of enantiomeric (3aRS,4RS,6aSR)-4-hydroxy-3,3a,4,6a-tetrahydro-1H-cyclopenta[c]furan-1-ones
2012 · Airat M. Gimazetdinov, Salavat S. Gataullin, et al. · Tetrahedron · 18
Simple synthetic protocol for the preparation of enantiomeric 3-oxabicyclo[3.3.0]oct-6-en-2-ones
2008 · Airat M. Gimazetdinov, Nikolay S. Vostrikov, et al. · Tetrahedron Asymmetry · 18
Simple antitumor model compounds for cross-conjugated cyclopentenone prostaglandins
2019 · Nikolay S. Vostrikov, Leonid V. Spirikhin, et al. · Mendeleev Communications · 11
A New Approach to the Synthesis of Chiral Blocks for Cyclopentanoids
2013 · Airat M. Gimazetdinov, Nadezhda A. Ivanova, et al. · Natural Product Communications · 11
Fluoride anion-induced intramolecular cyclopropanation of allylsilanes
2017 · Airat M. Gimazetdinov, Aidar Z. Al'mukhametov, et al. · Tetrahedron Letters · 8
New α-methylidenecyclopentenone block from Corey lactone diol
2013 · Airat M. Gimazetdinov, Lena A. Khalfitdinova, et al. · Mendeleev Communications · 7
Synthesis of (+)-didesmethylmethylenomycin A methyl ester
2013 · Airat M. Gimazetdinov, Salavat S. Gataullin, et al. · Tetrahedron · 7
Synthesis of enantiomeric cyclosarcomycins
2010 · Airat M. Gimazetdinov, Tat’yana V. Gimazetdinova, et al. · Mendeleev Communications · 7
Enantiopure vicinally trisubstituted all-cis-bis(hydroxymethyl)-cyclopentenols and their derivatives
2018 · Airat M. Gimazetdinov, Aidar Z. Almukhametov, et al. · Mendeleev Communications · 6
Synthetically attractive chiral cyclopentenone building blocks conjugated with tetrahydro- and 2-oxotetrahydrofurans
2018 · Aidar Z. Al’mukhametov, Airat M. Gimazetdinov, et al. · Mendeleev Communications · 5
Hydroxy-directed Prins cyclizations. Synthesis of the bowl-type chiral tricyclic cyclopentanoids, bicyclic pyranes, and furanes
2015 · Airat M. Gimazetdinov, Vladimir V. Loza, et al. · Tetrahedron Asymmetry · 5
Some aspects of the synthesis and modification of cross-conjugated cyclopentenone prostaglandins
2023 · A. M. Gimazetdinov, V. V. Zagitov, et al. · Russian Chemical Bulletin · 4
Development of a new approach for the synthesis of (+)-15-deoxy-Δ 12,14 -prostaglandin J 2 methyl ester based on the [2+2]-cycloadduct of 5-trimethylsilylcyclopentadiene and dichloroketene
2022 · Airat M. Gimazetdinov, Aidar Z. Al’mukhametov, et al. · New Journal of Chemistry · 4
A convenient synthesis of enantiopure (4aS,7aR)-1,4,4a,7a-tetrahydrocyclopenta[c]pyran-3,7-dione
2020 · Aidar Z. Al’mukhametov, Airat M. Gimazetdinov, et al. · Mendeleev Communications · 4
Sarkomycin A methyl esters and functionalized cyclopentane blocks for brefeldin A
2012 · A. M. Gimazetdinov, G. V. Ishmurzina, et al. · Russian Journal of Organic Chemistry · 4
Features of catalyzed hydration of 2-(dichloromethyl)-N-[(1R)-1-phenylethyl)]cyclopent-3-ene-1-carboxamides
2009 · A. M. Gizametdinov, M. S. Miftakhov · Russian Journal of Organic Chemistry · 4
Synthesis and Cytotoxic Properties of Cross-Conjugated Prostanoids with an exo-Methylidenecyclopentenone Fragment
2022 · A. Z. Al’mukhametov, G. V. Aralbaeva, et al. · Russian Journal of Organic Chemistry · 3
Formal synthesis of J-type prostaglandins based on enantiopure polyfunctional cyclopentenol derivative
2021 · Airat M. Gimazetdinov, Aidar Z. Al’mukhametov, et al. · Mendeleev Communications · 3
Synthetic Approaches to 15-Deoxy-Δ12,14-prostaglandin J2. A New Key Building Block Based on (3aR,6R,6aS)-6-Trimethylsilyl)-3,3a,6,6a-tetrahydro-1H-cyclopenta[c]furan-1-one
2019 · A. M. Gimazetdinov, A. Z. Al’mukhametov, et al. · Russian Journal of Organic Chemistry · 3
Some aspects of intramolecular carbocyclization of methyl (2E)-3-[(1S,2R,5R)-2-({[tert-butyl(dimethyl)-silyl]oxy}methyl)-5-(trimethylsilyl)cyclopent-3-en-1-yl]prop-2-enoate and its derivatives
2017 · A. M. Gimazetdinov, A. Z. Al’mukhametov, et al. · Russian Journal of Organic Chemistry · 3
New chiral block for cyclopentanoids synthesis
2016 · A. M. Gimazetdinov, V. Z. Almukhametov, et al. · Russian Journal of Organic Chemistry · 3
Enantiomeric 4,4a,7,7a-tetrahydro-1H-cyclopenta[c]pyran-3-ones
2009 · Airat M. Gimazetdinov, Tatyana V. Kolesnikova, et al. · Mendeleev Communications · 3
Epoxy derivatives of {(5-[(1-Phenylethyl)aminocarbonyl]-cyclopent-2-en-1-yl}methyl acetates
2010 · A. M. Gimazetdinov, M. S. Miftakhov · Russian Journal of Organic Chemistry · 2
Discriminatory silylation of hydroxymethyl and hydroxyethyl groups in the product of the Grieco lactone conversion. Approaches to the total synthesis of (±)-methylenolactocin
2025 · Z. R. Makaev, A. M. Gimazetdinov, et al. · Russian Chemical Bulletin · 1
Works count: 47
Citation count: 167
H-index: 7
I10-index: 5
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