C. Matassini

发表

A step forward towards sustainable aerobic alcohol oxidation: new and revised catalysts based on transition metals on solid supports

C. Parmeggiani, C. Matassini, F. Cardona, 2017 .

Glucocerebrosidase (GCase) activity modulation by 2-alkyl trihydroxypiperidines: Inhibition and pharmacological chaperoning.

P. Paoli, S. Giachetti, A. Morrone, 2020, Bioorganic chemistry.

Synthesis of “All-Cis” Trihydroxypiperidines from a Carbohydrate-Derived Ketone: Hints for the Design of New β-Gal and GCase Inhibitors

A. Morrone, C. Matassini, F. Cardona, 2020, Molecules.

Allyl Cyanate/Isocyanate Rearrangement in Glycals: Stereoselective Synthesis of 1-Amino and Diamino Sugar Derivatives

C. Matassini, F. Cardona, C. Faggi, 2020, Organic letters.

Multimerization of DAB-1 onto Au GNPs affords new potent and selective N-acetylgalactosamine-6-sulfatase (GALNS) inhibitors.

A. Morrone, C. Matassini, F. Cardona, 2018, Organic & biomolecular chemistry.

Gold nanoparticles are suitable cores for building tunable iminosugar multivalency

C. Parmeggiani, S. Penadés, C. Matassini, 2015 .

Mechanistic Insight into the Binding of Multivalent Pyrrolidines to α-Mannosidases.

C. Matassini, F. Cardona, I. Robina, 2017, Chemistry.

Piperidine Azasugars Bearing Lipophilic Chains: Stereoselective Synthesis and Biological Activity as Inhibitors of Glucocerebrosidase (GCase)

P. Merino, A. Morrone, C. Matassini, 2021, The Journal of organic chemistry.

Imino- and azasugar protonation inside human acid β-glucosidase, the enzyme defective in Gaucher disease.

M. Bols, A. Morrone, C. Matassini, 2020, Angewandte Chemie.

Imino‐ and Azasugar Protonation Inside Human Acid β‐Glucosidase, the Enzyme that is Defective in Gaucher Disease

M. Bols, A. Morrone, C. Matassini, 2020, Angewandte Chemie.

Human Acid β‐Glucosidase Inhibition by Carbohydrate Derived Iminosugars: Towards New Pharmacological Chaperones for Gaucher Disease

P. Paoli, C. Parmeggiani, A. Morrone, 2015, Chembiochem : a European journal of chemical biology.

Studies for the Multimerization of DAB-1-Based Iminosugars through Iteration of the Nitrone Cycloaddition/Ring-Opening/Allylation Sequence

C. Matassini, F. Cardona, A. Goti, 2019, European Journal of Organic Chemistry.

Synthesis of a New β-Galactosidase Inhibitor Displaying Pharmacological Chaperone Properties for GM1 Gangliosidosis

A. Morrone, C. Matassini, F. Cardona, 2022, Molecules.

GCase Enhancers: A Potential Therapeutic Option for Gaucher Disease and Other Neurological Disorders

C. Matassini, F. Cardona, F. Clemente, 2022, Pharmaceuticals.

Probing the Influence of Linker Length and Flexibility in the Design and Synthesis of New Trehalase Inhibitors

C. Matassini, F. Cardona, P. Parenti, 2018, Molecules.

Multivalent Resorcinarene Clusters Decorated with DAB-1 Inhitopes: Targeting Golgi α-Mannosidase from Drosophila Melanogaster

C. Gaeta, P. Neri, C. Matassini, 2021, Organic Chemistry Frontiers.

Double Reductive Amination and Selective Strecker Reaction of a D-Lyxaric Aldehyde: Synthesis of Diversely Functionalized 3,4,5-Trihydroxypiperidines

C. Matassini, F. Cardona, A. Goti, 2012 .

On the Virtue of Indium in Reduction Reactions. A Comparison of Reductions Mediated by Indium and Zinc: Is Indium Metal an Effective Catalyst for Zinc Induced Reductions?

S. Cicchi, C. Matassini, M. Marradi, 2019, European Journal of Inorganic Chemistry.

An Intramolecular Hydroaminomethylation-Based Approach to Pyrrolizidine Alkaloids under Microwave-Assisted Heating

M. Taddei, C. Matassini, F. Cardona, 2022, Molecules.

Reductive Amination Routes in the Synthesis of Piperidine IminoSugars

C. Matassini, F. Cardona, F. Clemente, 2020 .

Polyhydroxyamino‐Piperidine‐Type Iminosugars and Pipecolic Acid Analogues from a D‐Mannose‐Derived Aldehyde

C. Matassini, F. Cardona, I. Robina, 2014 .

New Frontiers on Human Safe Insecticides and Fungicides: An Opinion on Trehalase Inhibitors

C. Parmeggiani, C. Matassini, F. Cardona, 2020, Molecules.

On the Oxidation of Hydroxylamines with o-Iodoxybenzoic Acid (IBX)

C. Parmeggiani, C. Matassini, F. Cardona, 2017, Synthesis.

Evidence for a multivalent effect in inhibition of sulfatases involved in lysosomal storage disorders (LSDs)

P. Paoli, C. Parmeggiani, A. Morrone, 2016 .

Synthesis of Novel Iminosugar‐Based Trehalase Inhibitors by Cross‐Metathesis Reactions

C. Matassini, F. Cardona, D. Bini, 2011 .

Oxidation of N,N-Disubstituted Hydroxylamines to Nitrones with Hypervalent Iodine Reagents.

C. Parmeggiani, C. Matassini, F. Cardona, 2015, Organic letters.

Accessing 2-substituted piperidine iminosugars by organometallic addition/intramolecular reductive amination: aldehyde vs. nitrone route.

C. Matassini, F. Cardona, G. Fibbi, 2017, Organic & biomolecular chemistry.

Stereoselective Synthesis of C-2 Alkylated Trihydroxypiperidines: Novel Pharmacological Chaperones for Gaucher Disease.

P. Paoli, A. Morrone, C. Matassini, 2019, ACS medicinal chemistry letters.

Structural basis of the inhibition of GH1 beta-glucosidases by multivalent pyrrolidine iminosugars.

David Talens-Perales, J. Polaina, J. Sanz-Aparicio, 2019 .

Structural basis of the inhibition of GH1 β-glucosidases by multivalent pyrrolidine iminosugars.

David Talens-Perales, J. Polaina, J. Sanz-Aparicio, 2019, Bioorganic chemistry.

Hybrid Multivalent Jack Bean α-Mannosidase Inhibitors: The First Example of Gold Nanoparticles Decorated with Deoxynojirimycin Inhitopes

S. Moya, P. Compain, C. Matassini, 2021, Molecules.

Are enzymes sensitive to the multivalent effect? Emerging evidence with glycosidases

C. Parmeggiani, C. Matassini, F. Cardona, 2016 .

Dual targeting of PTP1B and glucosidases with new bifunctional iminosugar inhibitors to address type 2 diabetes.

P. Paoli, A. Morrone, C. Matassini, 2019, Bioorganic chemistry.

Synthesis of multimeric pyrrolidine iminosugar inhibitors of human β-glucocerebrosidase and α-galactosidase A: First example of a multivalent enzyme activity enhancer for Fabry disease.

C. Matassini, F. Cardona, I. Robina, 2020, European journal of medicinal chemistry.

Glycomimetic Based Approach toward Selective Carbonic Anhydrase Inhibitors.

C. Supuran, A. Angeli, C. Matassini, 2020, ACS medicinal chemistry letters.

Synthesis of Azasugar–Sulfonamide conjugates and their Evaluation as Inhibitors of Carbonic Anhydrases: the Azasugar Approach to Selectivity

C. Supuran, M. Ferraroni, A. Angeli, 2021 .

Carbohydrate Functionalized Quantum Dots in Sensing, Imaging and Therapy Applications

C. Matassini, M. Marradi, B. Richichi, 2020 .

Exploring architectures displaying multimeric presentations of a trihydroxypiperidine iminosugar

C. Matassini, F. Cardona, I. Robina, 2015, Beilstein Journal of Organic Chemistry.

Liquid Crystal‐Induced Myoblast Alignment

Piero Baglioni, Daniele Martella, Massimo Bonini, 2019, Advanced healthcare materials.

Mono- and three-tailed sugar and iminosugar decorated benzenesulfonamide carbonic anhydrase inhibitors.

C. Supuran, M. Ferraroni, A. Angeli, 2023, Organic & biomolecular chemistry.

Women in Bioorganic Chemistry

C. Parmeggiani, C. Matassini, F. Cardona, 2022, Molecules.