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Fernando Alberício

Researcher Next ID · RN-028450

Researcher · Biochemistry, Genetics and Molecular Biology

Barcelona Biomedical Research Park

Barcelona, South Africa

Not currently recruitingFunding unknown
Works count
1,342
Citation count
40,876
H-index
100
i10-index
717

Research interests

Biochemistry, Genetics and Molecular Biology
Chemistry
Immunology and Microbiology
Chemical Synthesis and Analysis
Click Chemistry and Applications
Carbohydrate Chemistry and Synthesis
Biochemical and Structural Characterization
Antimicrobial Peptides and Activities

Publications

  • Strategies for Improving Peptide Stability and Delivery

    Pharmaceuticals · 2022 · 10.3390/ph15101283

  • Chemical Approaches to the Synthesis of Peptides and Proteins

    · 2020 · 10.1201/9781003069225

  • The road to the synthesis of “difficult peptides”

    Chemical Society Reviews · 2015 · 10.1039/c5cs00680e

  • New peptide architectures through C–H activation stapling between tryptophan–phenylalanine/tyrosine residues

    Nature Communications · 2015 · 10.1038/ncomms8160

  • CuAAC: An Efficient Click Chemistry Reaction on Solid Phase

    ACS Combinatorial Science · 2015 · 10.1021/acscombsci.5b00087

  • Chemical Protein Synthesis Using a Second-Generation N-Acylurea Linker for the Preparation of Peptide-Thioester Precursors

    Journal of the American Chemical Society · 2015 · 10.1021/jacs.5b03504

  • Tetrahydrofuran-Containing Macrolides: A Fascinating Gift from the Deep Sea

    Chemical Reviews · 2013 · 10.1021/cr3004778

  • Multifaceted Roles of Disulfide Bonds. Peptides as Therapeutics

    Chemical Reviews · 2013 · https://doi.org/10.1021/cr400031z

  • Therapeutic Peptides

    Future Medicinal Chemistry · 2012 · 10.4155/fmc.12.94

  • Polymers and Drug Delivery Systems

    Current Drug Delivery · 2012 · 10.2174/156720112801323053

  • Peptide Coupling Reagents, More than a Letter Soup

    Chemical Reviews · 2011 · https://doi.org/10.1021/cr100048w

  • Structure, Bioactivity and Synthesis of Natural Products with Hexahydropyrrolo[2,3‐ b ]indole

    Chemistry - A European Journal · 2011 · 10.1002/chem.201001451

  • Targeted PLGA nano- but not microparticles specifically deliver antigen to human dendritic cells via DC-SIGN in vitro

    Journal of Controlled Release · 2010 · 10.1016/j.jconrel.2010.02.013

  • Oxyma: An Efficient Additive for Peptide Synthesis to Replace the Benzotriazole‐Based HOBt and HOAt with a Lower Risk of Explosion [1]

    Chemistry - A European Journal · 2009 · 10.1002/chem.200900614

  • Amino Acid-Protecting Groups

    Chemical Reviews · 2009 · https://doi.org/10.1021/cr800323s

  • Amphiphilic peptides and their cross-disciplinary role as building blocks for nanoscience

    Chemical Society Reviews · 2009 · 10.1039/b906701a

  • COMU: A Safer and More Effective Replacement for Benzotriazole‐Based Uronium Coupling Reagents

    Chemistry - A European Journal · 2009 · 10.1002/chem.200900615

  • ChemMatrix, a Poly(ethylene glycol)-Based Support for the Solid-Phase Synthesis of Complex Peptides

    Journal of Combinatorial Chemistry · 2006 · 10.1021/cc0600019

  • Peptide and Amide Bond-Containing Dendrimers

    Chemical Reviews · 2005 · 10.1021/cr030449l

  • Developments in peptide and amide synthesis

    Current Opinion in Chemical Biology · 2004 · 10.1016/j.cbpa.2004.03.002

  • Use of Onium Salt-Based Coupling Reagents in Peptide Synthesis1

    The Journal of Organic Chemistry · 1998 · 10.1021/jo980807y

  • Backbone Amide Linker (BAL) Strategy for Solid-Phase Synthesis of C-Terminal-Modified and Cyclic Peptides1,2,3

    Journal of the American Chemical Society · 1998 · 10.1021/ja974116f

  • Advantageous applications of azabenzotriazole (triazolopyridine)-based coupling reagents to solid-phase peptide synthesis

    Journal of the Chemical Society Chemical Communications · 1994 · 10.1039/c39940000201

  • A novel, convenient, three-dimensional orthogonal strategy for solid-phase synthesis of cyclic peptides

    Tetrahedron Letters · 1993 · 10.1016/0040-4039(93)85003-f

  • Preparation and application of the 5-(4-(9-fluorenylmethyloxycarbonyl)aminomethyl-3,5-dimethoxyphenoxy)-valeric acid (PAL) handle for the solid-phase synthesis of C-terminal peptide amides under mild conditions

    The Journal of Organic Chemistry · 1990 · 10.1021/jo00299a011

Current projects

    No projects listed.