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Differentiation between Isomeric 4,5-Functionalized 1,2,3-Thiadiazoles and 1,2,3-Triazoles by ESI-HRMS and IR Ion Spectroscopy

Molecules (Basel, Switzerland), 2023-01, Vol.28 (3), p.977

2023

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Synthesis, Fungicidal Activity and Plant Protective Properties of 1,2,3-Thiadiazole and Isothiazole-Based N -acyl- N -arylalaninates

Molecules (Basel, Switzerland), 2023-01, Vol.28 (1), p.419

2023

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[3+2] Anionic Cycloaddition of Isocyanides to Acyclic Enamines and Enaminones: A New, Simple, and Convenient Method for the Synthesis of 2,4‐Disubstituted Pyrroles

European journal of organic chemistry, 2020-03, Vol.2020 (9), p.1108-1113

2020

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Synthesis of Non-Aromatic Pyrroles Based on the Reaction of Carbonyl Derivatives of Acetylene with 3,3-Diaminoacrylonitriles

Molecules (Basel, Switzerland), 2023-04, Vol.28 (8), p.3576

2023

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Cyanothioacetamides as a synthetic platform for the synthesis of aminopyrazole derivatives

Beilstein journal of organic chemistry, 2023-08, Vol.19 (1), p.1191-1197

2023

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Higher-order QCD perturbation theory in different schemes: from FOPT to CIPT to FAPT

The journal of high energy physics, 2010-06, Vol.2010 (6), Article 85

2010

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Cycloaddition reactions of heterocyclic azides with 2-cyanoacetamidines as a new route to C , N -diheteroarylcarbamidines

Beilstein journal of organic chemistry, 2024, Vol.20 (1), p.17-24

2024

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Signaling Рathway Blockers: Action Mechanism, Efficacy, Safety of Therapy for Patients with Psoriasis and Psoriatic Arthritis

Vestnik dermatologij i venerologij, 2018-01, Vol.93 (5), p.89-96

Bakulev, A. A.

2018

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The Rich Chemistry Resulting from the 1,3‐Dipolar Cycloaddition Reactions of Enamines and Azides

European journal of organic chemistry, 2018-01, Vol.2018 (3), p.262-294

2018

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Design, Synthesis, and Evaluation of the Antifungal Activity of Novel Pyrazole–Thiazole Carboxamides as Succinate Dehydrogenase Inhibitors

Journal of agricultural and food chemistry, 2020-07, Vol.68 (27), p.7093-7102

2020

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Synthesis and properties of hydrazones bearing amide, thioamide and amidine functions

ARKIVOC, 2010-07, Vol.2010 (1), p.275-332

2010

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Selective Synthesis of Azoloyl NH-1,2,3-Triazoles and Azolyl Diazoketones: Experimental and Computational Insights

ACS omega, 2022-02, Vol.7 (6), p.5008-5031

2022

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Exploration of Fungicidal Activity and Mode of Action of Ferimzone Analogs

Journal of agricultural and food chemistry, 2023-03, Vol.71 (8), p.3705-3718

2023

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Synthesis of Coumarins Linked With 1,2,3-Triazoles under Microwave Irradiation and Evaluation of their Antimicrobial and Antioxidant Activity

Journal of the Mexican Chemical Society, 2020-01, Vol.64 (1), p.53-73

2020

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Evolution of the understanding of psoriasis and therapeutic approaches used to manage such patients. BCD-085 is the first Russian genetically-engineered biological preparation for the treatment of patients suffering from psoriasis

Vestnik dermatologij i venerologij, 2019-02, Vol.94 (5), p.26-32

Bakulev, A. L.

2019

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Rh(II)-mediated domino [4 + 1]-annulation of α-cyanothioacetamides using diazoesters: A new entry for the synthesis of multisubstituted thiophenes

Beilstein journal of organic chemistry, 2017-11, Vol.13 (1), p.2569-2576

2017

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Tandem Cycloaddition of Azides to 3,3-Diaminoacrylonitriles (2-Cyanoacetamidines) and Cornforth-Type Rearrangement as an Approach to 5‑Amino-1,2,3-triazole-4‑N‑substituted Imidamides

Journal of organic chemistry, 2023-07, Vol.88 (13), p.8163-8174

2023

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Synthesis, Fungicidal Activity, and Molecular Docking of 2‑Acylamino and 2‑Thioacylamino Derivatives of 1H‑benzo[d]imidazoles as Anti-Tubulin Agents

Journal of agricultural and food chemistry, 2021-10, Vol.69 (40), p.12048-12062

2021

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Rhodium-Catalyzed Transannulation of 4,5-Fused 1‑Sulfonyl-1,2,3-triazoles with Nitriles. The Selective Formation of 1‑Sulfonyl-4,5-fused Imidazoles versus Secondary C–H Bond Migration

Journal of organic chemistry, 2022-09, Vol.87 (18), p.12274-12286

2022

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Synthesis of 1,2,3-Thiadiazole and Thiazole-Based Strobilurins as Potent Fungicide Candidates

Journal of agricultural and food chemistry, 2017-02, Vol.65 (4), p.745-751

2017

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Combined experimental and theoretical studies of regio- and stereoselectivity in reactions of β-isoxazolyl- and β-imidazolyl enamines with nitrile oxides

Beilstein journal of organic chemistry, 2016-11, Vol.12 (1), p.2390-2401

2016

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A Base‐Controlled Reaction of 2‐Cyanoacetamidines (3,3‐Diaminoacrylonitriles) with Sulfonyl Azides as a Route to Nonaromatic 4‐Methylene‐1,2,3‐triazole‐5‐imines

European journal of organic chemistry, 2020-06, Vol.2020 (24), p.3688-3698

2020

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A facile access for the synthesis of 1-hetero(aryl)-1,2,3-triazoles linked to equol under mild conditions

Synthetic communications, 2020-10, Vol.50 (20), p.3086-3092

2020

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QCD-based pion distribution amplitudes confronting experimental data

Physics letters. B, 2001-05, Vol.508 (3), p.279-289

2001

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Suzuki-Miyaura coupling under microwave enhanced conditions: synthesis of 2-(hetero)aryl benzimidazoles

ARKIVOC free online journal of organic chemistry, 2020-02, Vol.2019 (6), p.431-445

2020

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Differentiation between Isomeric 4,5-Functionalized 1,2,3-Thiadiazoles and 1,2,3-Triazoles by ESI-HRMS and IR Ion Spectroscopy

Synthesis, Fungicidal Activity and Plant Protective Properties of 1,2,3-Thiadiazole and Isothiazole-Based N -acyl- N -arylalaninates

[3+2] Anionic Cycloaddition of Isocyanides to Acyclic Enamines and Enaminones: A New, Simple, and Convenient Method for the Synthesis of 2,4‐Disubstituted Pyrroles

Synthesis of Non-Aromatic Pyrroles Based on the Reaction of Carbonyl Derivatives of Acetylene with 3,3-Diaminoacrylonitriles

Cyanothioacetamides as a synthetic platform for the synthesis of aminopyrazole derivatives

Higher-order QCD perturbation theory in different schemes: from FOPT to CIPT to FAPT

Cycloaddition reactions of heterocyclic azides with 2-cyanoacetamidines as a new route to C , N -diheteroarylcarbamidines

Signaling Рathway Blockers: Action Mechanism, Efficacy, Safety of Therapy for Patients with Psoriasis and Psoriatic Arthritis

The Rich Chemistry Resulting from the 1,3‐Dipolar Cycloaddition Reactions of Enamines and Azides

Design, Synthesis, and Evaluation of the Antifungal Activity of Novel Pyrazole–Thiazole Carboxamides as Succinate Dehydrogenase Inhibitors

Synthesis and properties of hydrazones bearing amide, thioamide and amidine functions

Selective Synthesis of Azoloyl NH-1,2,3-Triazoles and Azolyl Diazoketones: Experimental and Computational Insights

Exploration of Fungicidal Activity and Mode of Action of Ferimzone Analogs

Synthesis of Coumarins Linked With 1,2,3-Triazoles under Microwave Irradiation and Evaluation of their Antimicrobial and Antioxidant Activity

Evolution of the understanding of psoriasis and therapeutic approaches used to manage such patients. BCD-085 is the first Russian genetically-engineered biological preparation for the treatment of patients suffering from psoriasis

Rh(II)-mediated domino [4 + 1]-annulation of α-cyanothioacetamides using diazoesters: A new entry for the synthesis of multisubstituted thiophenes

Tandem Cycloaddition of Azides to 3,3-Diaminoacrylonitriles (2-Cyanoacetamidines) and Cornforth-Type Rearrangement as an Approach to 5‑Amino-1,2,3-triazole-4‑N‑substituted Imidamides

Synthesis, Fungicidal Activity, and Molecular Docking of 2‑Acylamino and 2‑Thioacylamino Derivatives of 1H‑benzo[d]imidazoles as Anti-Tubulin Agents

Rhodium-Catalyzed Transannulation of 4,5-Fused 1‑Sulfonyl-1,2,3-triazoles with Nitriles. The Selective Formation of 1‑Sulfonyl-4,5-fused Imidazoles versus Secondary C–H Bond Migration

Synthesis of 1,2,3-Thiadiazole and Thiazole-Based Strobilurins as Potent Fungicide Candidates

Combined experimental and theoretical studies of regio- and stereoselectivity in reactions of β-isoxazolyl- and β-imidazolyl enamines with nitrile oxides

A Base‐Controlled Reaction of 2‐Cyanoacetamidines (3,3‐Diaminoacrylonitriles) with Sulfonyl Azides as a Route to Nonaromatic 4‐Methylene‐1,2,3‐triazole‐5‐imines

A facile access for the synthesis of 1-hetero(aryl)-1,2,3-triazoles linked to equol under mild conditions

QCD-based pion distribution amplitudes confronting experimental data

Suzuki-Miyaura coupling under microwave enhanced conditions: synthesis of 2-(hetero)aryl benzimidazoles

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