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Sterically Facilitated Intramolecular Nucleophilic NMe2 Group Substitution in the Synthesis of Fused Isoxazoles: Theoretical Study

Molecules (Basel, Switzerland), 2020-12, Vol.25 (24), p.5977

2020

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Biologically Active Echinulin-Related Indolediketopiperazines from the Marine Sediment-Derived Fungus Aspergillus niveoglaucus

Molecules (Basel, Switzerland), 2019-12, Vol.25 (1), p.61

2019

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Chiral Diselenophosphoric Acids for Ion Pair Catalysis: A Novel Approach to Enhance Both Proton Donating and Proton Accepting Properties

Chemistry : a European journal, 2024-08, Vol.30 (44), p.e202401793-n/a

2024

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Transition‐Metal‐Free Synthesis of 2‐Substituted Benzo[cd]Indoles via the Reaction of 1‐Halo‐8‐lithionaphthalenes with Nitriles

Chemistry : a European journal, 2024-02, Vol.30 (10), p.e202303768-n/a

2024

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The Role of Conjugation in the Halogen−Lithium Exchange Selectivity: Lithiation of 4,6,7,9‐Tetrabromo‐1,3‐dimethyl‐2,3‐dihydro‐1H‐perimidine

Chemistry : a European journal, 2023-08, Vol.29 (46), p.e202301439-n/a

2023

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NMR detection of the strained metallacycles in organolithiums: theoretical study

Organic & biomolecular chemistry, 2024-01, Vol.22 (5), p.982-989

2024

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Choice of computational protocol for carbon-lithium spin-spin coupling constants 1 J CLi

Magnetic resonance in chemistry, 2022-10, Vol.60 (10), p.985-995

2022

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Lithiation of 2,4,5,7-Tetrabromo-1,8-bis(dimethylamino)naphthalene: Peculiarities of Directing Groups’ Effects and the Possibility of Polymetalation

Organometallics, 2021-11, Vol.40 (21), p.3627-3636

2021

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Aggregation Behavior of Lithionaphthalenes in Solution: Experimental and Theoretical Study

Organometallics, 2020-10, Vol.39 (20), p.3705-3714

2020

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Organometallic Synthesis of 2,3,6,7-Tetrasubstituted 1,8-Bis(dimethylamino)naphthalenes for Investigation of the Double Buttressing Effect in Proton Sponges

Journal of organic chemistry, 2022-12, Vol.87 (24), p.16506-16516

2022

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Spontaneous Cyclization of peri-Diiminonaphthalenes Leading to the Formation of Benzo[de]isoquinolines and Stable Benzo[de]isoquinoliniums

Organic letters, 2023-02, Vol.25 (6), p.977-981

2023

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Choice of computational protocol for carbon‐lithium spin–spin coupling constants 1JCLi

Magnetic resonance in chemistry, 2022-10, Vol.60 (10), p.985-995

2022

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Phosphine selenides: versatile NMR probes for analyzing hydrogen OH⋯Se and halogen I⋯Se bonds

Physical chemistry chemical physics : PCCP, 2024-09, Vol.26 (37), p.24488-24497

2024

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Tandem Synthesis of 10-Dimethylaminobenzo[h]quinazolines from 2‑Ketimino-1,8-bis(dimethylamino)naphthalenes via Nucleophilic Replacement of the Unactivated Aromatic NMe2 Group

Organic letters, 2016-06, Vol.18 (12), p.2872-2875

2016

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“Buttressing Effect” in the Halogen‐Lithium Exchange in ortho‐Bromo‐N,N‐dimethylanilines and Related Naphthalenes

Chemistry : a European journal, 2024-03, Vol.30 (14), p.e202303956-n/a

2024

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peri -Interactions in 1,8-bis(dimethylamino)naphthalene ortho -ketimine cations facilitate [1,5]-hydride shift: selective synthesis of 1,2,3,4-tetrahydrobenzo[ h ]quinazolines

Organic & biomolecular chemistry, 2022-06, Vol.20 (22), p.4559-4568

2022

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αVβ3 integrin regulates macrophage inflammatory responses via PI3 kinase/Akt-dependent NF-κB activation

Journal of cellular physiology, 2011-02, Vol.226 (2), p.469-476

2011

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Self-association of diphenylpnictoginic acids in solution and solid state: covalent vs. hydrogen bonding

Physical chemistry chemical physics : PCCP, 2022-03, Vol.24 (13), p.7882-7892

2022

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How Strong is Hydrogen Bonding to Amide Nitrogen?

Chemphyschem, 2020-04, Vol.21 (7), p.651-658

2020

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Proton-induced fluorescence in modified quino[7,8-]quinolines: dual sensing for protons and π-donors

Organic & biomolecular chemistry, 2019-09, Vol.17 (35), p.8221-8233

2019

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10-Dimethylamino Derivatives of Benzo[h]quinoline and Benzo[h]quinazolines: Fluorescent Proton Sponge Analogues with Opposed peri-NMe2/–N Groups. How to Distinguish between Proton Sponges and Pseudo-Proton Sponges

Journal of organic chemistry, 2016-07, Vol.81 (13), p.5574-5587

2016

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Out-basicity of 1,8-bis(dimethylamino)naphthalene: the experimental and theoretical challenge

Organic & biomolecular chemistry, 2014-04, Vol.12 (15), p.2360-2369

2014

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Naphto-Γ-pyrones from the marine-derived fungus Aspergillus foetidus

Natural product research, 2021, Vol.35 (1), p.131-134

2021

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Ring lithiation of 1,8-bis(dimethylamino)naphthalene: another side of the 'proton sponge coin'

Dalton transactions : an international journal of inorganic chemistry, 2015-01, Vol.44 (40), p.17756-17766

2015

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Symmetry/Asymmetry of the NHN Hydrogen Bond in Protonated 1,8-Bis(dimethylamino)naphthalene

Symmetry (Basel), 2020-11, Vol.12 (11), p.1924

2020

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Sterically Facilitated Intramolecular Nucleophilic NMe2 Group Substitution in the Synthesis of Fused Isoxazoles: Theoretical Study

Biologically Active Echinulin-Related Indolediketopiperazines from the Marine Sediment-Derived Fungus Aspergillus niveoglaucus

Chiral Diselenophosphoric Acids for Ion Pair Catalysis: A Novel Approach to Enhance Both Proton Donating and Proton Accepting Properties

Transition‐Metal‐Free Synthesis of 2‐Substituted Benzo[cd]Indoles via the Reaction of 1‐Halo‐8‐lithionaphthalenes with Nitriles

The Role of Conjugation in the Halogen−Lithium Exchange Selectivity: Lithiation of 4,6,7,9‐Tetrabromo‐1,3‐dimethyl‐2,3‐dihydro‐1H‐perimidine

NMR detection of the strained metallacycles in organolithiums: theoretical study

Choice of computational protocol for carbon-lithium spin-spin coupling constants 1 J CLi

Lithiation of 2,4,5,7-Tetrabromo-1,8-bis(dimethylamino)naphthalene: Peculiarities of Directing Groups’ Effects and the Possibility of Polymetalation

Aggregation Behavior of Lithionaphthalenes in Solution: Experimental and Theoretical Study

Organometallic Synthesis of 2,3,6,7-Tetrasubstituted 1,8-Bis(dimethylamino)naphthalenes for Investigation of the Double Buttressing Effect in Proton Sponges

Spontaneous Cyclization of peri-Diiminonaphthalenes Leading to the Formation of Benzo[de]isoquinolines and Stable Benzo[de]isoquinoliniums

Choice of computational protocol for carbon‐lithium spin–spin coupling constants 1JCLi

Phosphine selenides: versatile NMR probes for analyzing hydrogen OH⋯Se and halogen I⋯Se bonds

Tandem Synthesis of 10-Dimethylaminobenzo[h]quinazolines from 2‑Ketimino-1,8-bis(dimethylamino)naphthalenes via Nucleophilic Replacement of the Unactivated Aromatic NMe2 Group

“Buttressing Effect” in the Halogen‐Lithium Exchange in ortho‐Bromo‐N,N‐dimethylanilines and Related Naphthalenes

peri -Interactions in 1,8-bis(dimethylamino)naphthalene ortho -ketimine cations facilitate [1,5]-hydride shift: selective synthesis of 1,2,3,4-tetrahydrobenzo[ h ]quinazolines

αVβ3 integrin regulates macrophage inflammatory responses via PI3 kinase/Akt-dependent NF-κB activation

Self-association of diphenylpnictoginic acids in solution and solid state: covalent vs. hydrogen bonding

How Strong is Hydrogen Bonding to Amide Nitrogen?

Proton-induced fluorescence in modified quino[7,8-]quinolines: dual sensing for protons and π-donors

10-Dimethylamino Derivatives of Benzo[h]quinoline and Benzo[h]quinazolines: Fluorescent Proton Sponge Analogues with Opposed peri-NMe2/–N Groups. How to Distinguish between Proton Sponges and Pseudo-Proton Sponges

Out-basicity of 1,8-bis(dimethylamino)naphthalene: the experimental and theoretical challenge

Naphto-Γ-pyrones from the marine-derived fungus Aspergillus foetidus

Ring lithiation of 1,8-bis(dimethylamino)naphthalene: another side of the 'proton sponge coin'

Symmetry/Asymmetry of the NHN Hydrogen Bond in Protonated 1,8-Bis(dimethylamino)naphthalene

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