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SARS-CoV-2 Mpro: A Potential Target for Peptidomimetics and Small-Molecule Inhibitors

Biomolecules (Basel, Switzerland), 2021-04, Vol.11 (4), p.607

2021

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Peptidyl Fluoromethyl Ketones and Their Applications in Medicinal Chemistry

Molecules (Basel, Switzerland), 2020-09, Vol.25 (17), p.4031

2020

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Cyrene: A Green Solvent for the Synthesis of Bioactive Molecules and Functional Biomaterials

International journal of molecular sciences, 2022-12, Vol.23 (24), p.15960

2022

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Hydroxamic Acid Derivatives: From Synthetic Strategies to Medicinal Chemistry Applications

ACS omega, 2021-08, Vol.6 (34), p.21843-21849

2021

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Syntheses, reactivity, and biological applications of coumarins

Frontiers in chemistry, 2024-02, Vol.12, p.1362992-1362992

2024

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Natural Product-Based Hybrids as Potential Candidates for the Treatment of Cancer: Focus on Curcumin and Resveratrol

Molecules (Basel, Switzerland), 2021-07, Vol.26 (15), p.4665

2021

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Hydrogels for the Delivery of Plant-Derived (Poly)Phenols

Molecules (Basel, Switzerland), 2020-07, Vol.25 (14), p.3254

2020

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Nano-Formulations of Natural Antioxidants for the Treatment of Liver Cancer

Biomolecules (Basel, Switzerland), 2024-08, Vol.14 (8), p.1031

2024

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Recent Advances in SARS-CoV-2 Main Protease Inhibitors: From Nirmatrelvir to Future Perspectives

Biomolecules (Basel, Switzerland), 2023-09, Vol.13 (9), p.1339

2023

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Hydroxamic Acid-Based Histone Deacetylase (HDAC) Inhibitors Bearing a Pyrazole Scaffold and a Cinnamoyl Linker

International journal of molecular sciences, 2019-02, Vol.20 (4), p.945

2019

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Pseudo-Dipeptide Bearing α,α-Difluoromethyl Ketone Moiety as Electrophilic Warhead with Activity against Coronaviruses

International journal of molecular sciences, 2021-01, Vol.22 (3), p.1398

2021

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Novel Class of Proteasome Inhibitors: In Silico and In Vitro Evaluation of Diverse Chloro(trifluoromethyl)aziridines

International journal of molecular sciences, 2022-10, Vol.23 (20), p.12363

2022

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Computational Design, Synthesis, and Biophysical Evaluation of β-Amido Boronic Acids as SARS-CoV-2 Mpro Inhibitors

Molecules (Basel, Switzerland), 2023-03, Vol.28 (5), p.2356

2023

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Discovery of a Novel Trifluoromethyl Diazirine Inhibitor of SARS-CoV-2 Mpro

Molecules (Basel, Switzerland), 2023-01, Vol.28 (2), p.514

2023

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Direct and Chemoselective Synthesis of Tertiary Difluoroketones via Weinreb Amide Homologation with a CHF2‑Carbene Equivalent

Organic letters, 2019-10, Vol.21 (20), p.8261-8265

2019

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Dual Targeting Strategies on Histone Deacetylase 6 (HDAC6) and Heat Shock Protein 90 (Hsp90)

Current medicinal chemistry, 2022-03, Vol.29 (9), p.1474-1502

2022

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Chemoselective Homologation–Deoxygenation Strategy Enabling the Direct Conversion of Carbonyls into (n+1)‑Halomethyl-Alkanes

Organic letters, 2020-10, Vol.22 (19), p.7629-7634

2020

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A Green Approach to Nucleophilic Aromatic Substitutions of Nicotinic Esters in Cyrene

European journal of organic chemistry, 2024-04, Vol.27 (15)

2024

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Front Cover: A Green Approach to Nucleophilic Aromatic Substitutions of Nicotinic Esters in Cyrene (Eur. J. Org. Chem. 15/2024)

European journal of organic chemistry, 2024-04, Vol.27 (15)

2024

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Synthesis, computational investigation and biological evaluation of α,α-difluoromethyl ketones embodying pyrazole and isoxazole nuclei as COX inhibitors

Organic & biomolecular chemistry, 2022-11, Vol.2 (42), p.8293-834

2022

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Discovery of potent pyrrolo-pyrimidine and purine HDAC inhibitors for the treatment of advanced prostate cancer

European journal of medicinal chemistry, 2023-11, Vol.260, p.115730, Article 115730

2023

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First total synthesis of caerulomycin K: a case study on selective, multiple C-H functionalizations of pyridines

RSC advances, 2024-02, Vol.14 (8), p.5542-5546

2024

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Synthesis of potent and selective HDAC6 inhibitors led to unexpected opening of a quinazoline ring

RSC advances, 2022-04, Vol.12 (18), p.11548-11556

2022

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Direct and Chemoselective Synthesis of Tertiary Difluoroketones via Weinreb Amide Homologation with a CHF 2 -Carbene Equivalent

Organic letters, 2019-10, Vol.21 (20), p.8261-8265

2019

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Selective noncovalent proteasome inhibiting activity of trifluoromethyl‐containing gem‐quaternary aziridines

Archiv der Pharmazie (Weinheim), 2023-07, Vol.356 (7), p.e2300174-n/a

2023

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SARS-CoV-2 Mpro: A Potential Target for Peptidomimetics and Small-Molecule Inhibitors

Peptidyl Fluoromethyl Ketones and Their Applications in Medicinal Chemistry

Cyrene: A Green Solvent for the Synthesis of Bioactive Molecules and Functional Biomaterials

Hydroxamic Acid Derivatives: From Synthetic Strategies to Medicinal Chemistry Applications

Syntheses, reactivity, and biological applications of coumarins

Natural Product-Based Hybrids as Potential Candidates for the Treatment of Cancer: Focus on Curcumin and Resveratrol

Hydrogels for the Delivery of Plant-Derived (Poly)Phenols

Nano-Formulations of Natural Antioxidants for the Treatment of Liver Cancer

Recent Advances in SARS-CoV-2 Main Protease Inhibitors: From Nirmatrelvir to Future Perspectives

Hydroxamic Acid-Based Histone Deacetylase (HDAC) Inhibitors Bearing a Pyrazole Scaffold and a Cinnamoyl Linker

Pseudo-Dipeptide Bearing α,α-Difluoromethyl Ketone Moiety as Electrophilic Warhead with Activity against Coronaviruses

Novel Class of Proteasome Inhibitors: In Silico and In Vitro Evaluation of Diverse Chloro(trifluoromethyl)aziridines

Computational Design, Synthesis, and Biophysical Evaluation of β-Amido Boronic Acids as SARS-CoV-2 Mpro Inhibitors

Discovery of a Novel Trifluoromethyl Diazirine Inhibitor of SARS-CoV-2 Mpro

Direct and Chemoselective Synthesis of Tertiary Difluoroketones via Weinreb Amide Homologation with a CHF2‑Carbene Equivalent

Dual Targeting Strategies on Histone Deacetylase 6 (HDAC6) and Heat Shock Protein 90 (Hsp90)

Chemoselective Homologation–Deoxygenation Strategy Enabling the Direct Conversion of Carbonyls into (n+1)‑Halomethyl-Alkanes

A Green Approach to Nucleophilic Aromatic Substitutions of Nicotinic Esters in Cyrene

Front Cover: A Green Approach to Nucleophilic Aromatic Substitutions of Nicotinic Esters in Cyrene (Eur. J. Org. Chem. 15/2024)

Synthesis, computational investigation and biological evaluation of α,α-difluoromethyl ketones embodying pyrazole and isoxazole nuclei as COX inhibitors

Discovery of potent pyrrolo-pyrimidine and purine HDAC inhibitors for the treatment of advanced prostate cancer

First total synthesis of caerulomycin K: a case study on selective, multiple C-H functionalizations of pyridines

Synthesis of potent and selective HDAC6 inhibitors led to unexpected opening of a quinazoline ring

Direct and Chemoselective Synthesis of Tertiary Difluoroketones via Weinreb Amide Homologation with a CHF 2 -Carbene Equivalent

Selective noncovalent proteasome inhibiting activity of trifluoromethyl‐containing gem‐quaternary aziridines

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