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Biologically active compounds based on the privileged 2-imidazoline scaffold: The world beyond adrenergic/imidazoline receptor modulators

European journal of medicinal chemistry, 2015-06, Vol.97, p.525-537

Krasavin, Mikhail

2015

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Spirocyclic Motifs in Natural Products

Molecules (Basel, Switzerland), 2019-11, Vol.24 (22), p.4165

2019

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Synthetic Studies towards CH‐Diazomethane Sulfonamides: a Novel Type of Diazo Reagents

European journal of organic chemistry, 2020-07, Vol.2020 (27), p.4112-4115

2020

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Multicomponent Reactions Involving Diazo Reagents: A 5-Year Update

Molecules (Basel, Switzerland), 2021-10, Vol.26 (21), p.6563

2021

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Antimicrobial Activity of 5-membered Nitroheteroaromatic Compounds beyond Nitrofurans and Nitroimidazoles: Recent Progress

Current medicinal chemistry, 2021-01, Vol.28 (29), p.5926-5982

2021

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Diazocarbonyl and Related Compounds in the Synthesis of Azoles

Molecules (Basel, Switzerland), 2021-04, Vol.26 (9), p.2530

2021

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Conjugates of Iron-Transporting N-Hydroxylactams with Ciprofloxacin

Molecules (Basel, Switzerland), 2022-06, Vol.27 (12), p.3910

2022

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Synthesis of spirocyclic tetrahydroisoquinolines (spiroTHIQs) via the Castagnoli-Cushman reaction

Tetrahedron letters, 2020-10, Vol.61 (42), p.152408, Article 152408

2020

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Exploration of Spirocyclic Derivatives of Ciprofloxacin as Antibacterial Agents

Molecules (Basel, Switzerland), 2022-07, Vol.27 (15), p.4864

2022

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A novel approach to biologically relevant oxazolo[5,4-d]pyrimidine-5,7-diones via readily available diazobarbituric acid derivatives

Tetrahedron letters, 2019-10, Vol.60 (44), p.151120, Article 151120

2019

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Carbonic Anhydrase IX Inhibitors as Candidates for Combination Therapy of Solid Tumors

International journal of molecular sciences, 2021-12, Vol.22 (24), p.13405

2021

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Preparation and Synthetic Applications of Five-to-Seven-Membered Cyclic α-Diazo Monocarbonyl Compounds

Molecules (Basel, Switzerland), 2022-03, Vol.27 (6), p.2030

2022

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The Use of Aryl-Substituted Homophthalic Anhydrides in the Castagnoli-Cushman Reaction Provides Access to Novel Tetrahydroisoquinolone Carboxylic Acid Bearing an All-Carbon Quaternary Stereogenic Center

Molecules (Basel, Switzerland), 2022-12, Vol.27 (23), p.8462

2022

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One-Pot Sequence of Staudinger/aza-Wittig/Castagnoli-Cushman Reactions Provides Facile Access to Novel Natural-like Polycyclic Ring Systems

Molecules (Basel, Switzerland), 2022-11, Vol.27 (23), p.8130

2022

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Extending the Scope of the New Variant of the Castagnoli–Cushman Cyclocondensation onto o-Methyl Benzoic Acids Bearing Various Electron-Withdrawing Groups in the α-Position

Molecules (Basel, Switzerland), 2022-10, Vol.27 (21), p.7211

2022

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Synthesis and Antibacterial Evaluation of Ciprofloxacin Congeners with Spirocyclic Amine Periphery

International journal of molecular sciences, 2023-01, Vol.24 (2), p.954

2023

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Inhibitory activity against carbonic anhydrase IX and XII as a candidate selection criterion in the development of new anticancer agents

Journal of enzyme inhibition and medicinal chemistry, 2020-01, Vol.35 (1), p.1555-1561

2020

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N-Arylation of Amidines and Guanidines: An Update

Current organic chemistry, 2016-06, Vol.20 (13), p.1370-1388

2016

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Dicarboxylic Acid Monoesters in β- and δ-Lactam Synthesis

Molecules (Basel, Switzerland), 2022-04, Vol.27 (8), p.2469

2022

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Facile and diastereoselective arylation of the privileged 1,4-dihydroisoquinolin-3(2 H )-one scaffold

Beilstein journal of organic chemistry, 2022-08, Vol.18 (1), p.1070-1078

2022

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Pd-Catalyzed N-arylation of 2-imidazolines Provides Convenient Access to Selective Cyclooxygenase-2 Inhibitors

Letters in organic chemistry, 2013-05, Vol.10 (4), p.235-239

Krasavin, Mikhail

2013

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Two Annulated Azaheterocyclic Cores Readily Available from a Single Tetrahydroisoquinolonic Castagnoli-Cushman Precursor

Molecules (Basel, Switzerland), 2020-04, Vol.25 (9), p.2049

2020

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Sulfocoumarins as dual inhibitors of human carbonic anhydrase isoforms IX/XII and of human thioredoxin reductase

Journal of enzyme inhibition and medicinal chemistry, 2020-01, Vol.35 (1), p.506-510

2020

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Facile Access to Fe(III)-Complexing Cyclic Hydroxamic Acids in a Three-Component Format

Molecules (Basel, Switzerland), 2019-02, Vol.24 (5), p.864

2019

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Biologically active compounds based on the privileged 2-imidazoline scaffold: The world beyond adrenergic/imidazoline receptor modulators

Spirocyclic Motifs in Natural Products

Synthetic Studies towards CH‐Diazomethane Sulfonamides: a Novel Type of Diazo Reagents

Multicomponent Reactions Involving Diazo Reagents: A 5-Year Update

Antimicrobial Activity of 5-membered Nitroheteroaromatic Compounds beyond Nitrofurans and Nitroimidazoles: Recent Progress

Diazocarbonyl and Related Compounds in the Synthesis of Azoles

Conjugates of Iron-Transporting N-Hydroxylactams with Ciprofloxacin

Synthesis of spirocyclic tetrahydroisoquinolines (spiroTHIQs) via the Castagnoli-Cushman reaction

Exploration of Spirocyclic Derivatives of Ciprofloxacin as Antibacterial Agents

Discovery of 2‑[1-(4,4-Difluorocyclohexyl)piperidin-4-yl]-6-fluoro-3-oxo-2,3-dihydro‑1H‑isoindole-4-carboxamide (NMS-P118): A Potent, Orally Available, and Highly Selective PARP‑1 Inhibitor for Cancer Therapy

A novel approach to biologically relevant oxazolo[5,4-d]pyrimidine-5,7-diones via readily available diazobarbituric acid derivatives

Carbonic Anhydrase IX Inhibitors as Candidates for Combination Therapy of Solid Tumors

Preparation and Synthetic Applications of Five-to-Seven-Membered Cyclic α-Diazo Monocarbonyl Compounds

The Use of Aryl-Substituted Homophthalic Anhydrides in the Castagnoli-Cushman Reaction Provides Access to Novel Tetrahydroisoquinolone Carboxylic Acid Bearing an All-Carbon Quaternary Stereogenic Center

One-Pot Sequence of Staudinger/aza-Wittig/Castagnoli-Cushman Reactions Provides Facile Access to Novel Natural-like Polycyclic Ring Systems

Extending the Scope of the New Variant of the Castagnoli–Cushman Cyclocondensation onto o-Methyl Benzoic Acids Bearing Various Electron-Withdrawing Groups in the α-Position

Synthesis and Antibacterial Evaluation of Ciprofloxacin Congeners with Spirocyclic Amine Periphery

Inhibitory activity against carbonic anhydrase IX and XII as a candidate selection criterion in the development of new anticancer agents

N-Arylation of Amidines and Guanidines: An Update

Dicarboxylic Acid Monoesters in β- and δ-Lactam Synthesis

Facile and diastereoselective arylation of the privileged 1,4-dihydroisoquinolin-3(2 H )-one scaffold

Pd-Catalyzed N-arylation of 2-imidazolines Provides Convenient Access to Selective Cyclooxygenase-2 Inhibitors

Two Annulated Azaheterocyclic Cores Readily Available from a Single Tetrahydroisoquinolonic Castagnoli-Cushman Precursor

Sulfocoumarins as dual inhibitors of human carbonic anhydrase isoforms IX/XII and of human thioredoxin reductase

Facile Access to Fe(III)-Complexing Cyclic Hydroxamic Acids in a Three-Component Format

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