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The Road from Host-Defense Peptides to a New Generation of Antimicrobial Drugs

Molecules (Basel, Switzerland), 2018-02, Vol.23 (2), p.311

2018

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Host-Defense Peptides as New Generation Phytosanitaries: Low Toxicity and Low Induction of Antimicrobial Resistance

Agronomy (Basel), 2022-07, Vol.12 (7), p.1614

2022

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Pure Organic Active Compounds Against Abiotic Stress: A Biostimulant Overview

Frontiers in plant science, 2020-12, Vol.11, p.575829

2020

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Prediction of Antifungal Activity of Antimicrobial Peptides by Transfer Learning from Protein Pretrained Models

International journal of molecular sciences, 2023-06, Vol.24 (12), p.10270

2023

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Site-selective modification of peptide backbones

Organic Chemistry Frontiers, 2021-11, Vol.8 (23), p.6720-6759

2021

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Microwave versus Conventional Light Activation of O‐Radical Scission Processes

European journal of organic chemistry, 2017-01, Vol.2017 (2), p.373-380

2017

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TBS-pyrrole as an “universal” reference to quantify artemisinin and structurally-diverse natural products in plants extracts by NMR

Frontiers in plant science, 2023-09, Vol.14, p.1255512-1255512

2023

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The use of chitosan oligosaccharide to improve artemisinin yield in well-watered and drought-stressed plants

Frontiers in plant science, 2023, Vol.14, p.1200898-1200898

2023

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FLTX2: A Novel Tamoxifen Derivative Endowed with Antiestrogenic, Fluorescent, and Photosensitizer Properties

International journal of molecular sciences, 2021-05, Vol.22 (10), p.5339

2021

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"Cut and Paste" Processes in the Search of Bioactive Products: One-Pot, Metal-free O -Radical Scission-Oxidation-Addition of C , N or P -Nucleophiles

Frontiers in chemistry, 2022-05, Vol.10, p.884124-884124

2022

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Simplification of antitumoral phenanthroindolizidine alkaloids: Short synthesis of cytotoxic indolizidinone and pyrrolidine analogs

European journal of medicinal chemistry, 2013-08, Vol.66, p.540-554

2013

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Short and Efficient Synthesis of Chiral Furyl Carbinols from Carbohydrates

Organic letters, 2007-04, Vol.9 (9), p.1721-1724

2007

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Domino Process Achieves Site-Selective Peptide Modification with High Optical Purity. Applications to Chain Diversification and Peptide Ligation

Journal of organic chemistry, 2015-10, Vol.80 (19), p.9379-9391

2015

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Conversion of Hydroxyproline “Doubly Customizable Units” to Hexahydropyrimidines: Access to Conformationally Constrained Peptides

Journal of organic chemistry, 2023-07, Vol.88 (14), p.9910-9919

2023

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One-Pot Synthesis of Acyclic Nucleosides from Carbohydrate Derivatives, by Combination of Tandem and Sequential Reactions

Journal of organic chemistry, 2007-12, Vol.72 (25), p.9523-9532

2007

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“Doubly Customizable” Unit for the Generation of Structural Diversity: From Pure Enantiomeric Amines to Peptide Derivatives

Journal of organic chemistry, 2021-02, Vol.86 (3), p.2796-2809

2021

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Structural diversity using amino acid “Customizable Units”: conversion of hydroxyproline (Hyp) into nitrogen heterocycles

Amino acids, 2022-06, Vol.54 (6), p.955-966

2022

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Creating Diversity by Site-Selective Peptide Modification: A Customizable Unit Affords Amino Acids with High Optical Purity

Organic letters, 2013-11, Vol.15 (22), p.5778-5781

2013

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Metal-Free, Site-Selective Peptide Modification by Conversion of "Customizable" Units into [beta]-Substituted Dehydroamino Acids

Chemistry : a European journal, 2018-01, Vol.24 (3), p.599

2018

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Frontispiece: Metal-Free, Site-Selective Peptide Modification by Conversion of "Customizable" Units into [beta]-Substituted Dehydroamino Acids

Chemistry : a European journal, 2018-01, Vol.24 (3)

2018

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Frontispiece: Metal‐Free, Site‐Selective Peptide Modification by Conversion of “Customizable” Units into β‐Substituted Dehydroamino Acids

Chemistry : a European journal, 2018-01, Vol.24 (3), p.n/a

2018

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Nucleoside Analogues: Synthesis and Biological Properties of Azanucleoside Derivatives

European journal of organic chemistry, 2014-04, Vol.2014 (11), p.2201-2220

2014

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Conversion of “Customizable Units” into N‑Alkyl Amino Acids and Generation of N‑Alkyl Peptides

Journal of organic chemistry, 2019-07, Vol.84 (13), p.8392-8410

2019

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Synthesis of Diketopiperazine Scaffolds with Tailored N‐ and α‐Chains by Selective Modification of Customizable Units

Advanced synthesis & catalysis, 2020-08, Vol.362 (15), p.3158-3169

2020

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Metal‐Free, Site‐Selective Peptide Modification by Conversion of “Customizable” Units into β‐Substituted Dehydroamino Acids

Chemistry : a European journal, 2018-01, Vol.24 (3), p.599-607

2018

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The Road from Host-Defense Peptides to a New Generation of Antimicrobial Drugs

Host-Defense Peptides as New Generation Phytosanitaries: Low Toxicity and Low Induction of Antimicrobial Resistance

Pure Organic Active Compounds Against Abiotic Stress: A Biostimulant Overview

Prediction of Antifungal Activity of Antimicrobial Peptides by Transfer Learning from Protein Pretrained Models

Site-selective modification of peptide backbones

Microwave versus Conventional Light Activation of O‐Radical Scission Processes

TBS-pyrrole as an “universal” reference to quantify artemisinin and structurally-diverse natural products in plants extracts by NMR

The use of chitosan oligosaccharide to improve artemisinin yield in well-watered and drought-stressed plants

FLTX2: A Novel Tamoxifen Derivative Endowed with Antiestrogenic, Fluorescent, and Photosensitizer Properties

"Cut and Paste" Processes in the Search of Bioactive Products: One-Pot, Metal-free O -Radical Scission-Oxidation-Addition of C , N or P -Nucleophiles

Simplification of antitumoral phenanthroindolizidine alkaloids: Short synthesis of cytotoxic indolizidinone and pyrrolidine analogs

Short and Efficient Synthesis of Chiral Furyl Carbinols from Carbohydrates

Domino Process Achieves Site-Selective Peptide Modification with High Optical Purity. Applications to Chain Diversification and Peptide Ligation

Conversion of Hydroxyproline “Doubly Customizable Units” to Hexahydropyrimidines: Access to Conformationally Constrained Peptides

One-Pot Synthesis of Acyclic Nucleosides from Carbohydrate Derivatives, by Combination of Tandem and Sequential Reactions

“Doubly Customizable” Unit for the Generation of Structural Diversity: From Pure Enantiomeric Amines to Peptide Derivatives

Structural diversity using amino acid “Customizable Units”: conversion of hydroxyproline (Hyp) into nitrogen heterocycles

Creating Diversity by Site-Selective Peptide Modification: A Customizable Unit Affords Amino Acids with High Optical Purity

Metal-Free, Site-Selective Peptide Modification by Conversion of "Customizable" Units into [beta]-Substituted Dehydroamino Acids

Frontispiece: Metal-Free, Site-Selective Peptide Modification by Conversion of "Customizable" Units into [beta]-Substituted Dehydroamino Acids

Frontispiece: Metal‐Free, Site‐Selective Peptide Modification by Conversion of “Customizable” Units into β‐Substituted Dehydroamino Acids

Nucleoside Analogues: Synthesis and Biological Properties of Azanucleoside Derivatives

Conversion of “Customizable Units” into N‑Alkyl Amino Acids and Generation of N‑Alkyl Peptides

Synthesis of Diketopiperazine Scaffolds with Tailored N‐ and α‐Chains by Selective Modification of Customizable Units

Metal‐Free, Site‐Selective Peptide Modification by Conversion of “Customizable” Units into β‐Substituted Dehydroamino Acids

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