Claudio Daniel Navo Nájera-rekin lankidetzan egindako argitalpenak (9)

2022

  1. Synthesis of β2,2-Amino Acids by Stereoselective Alkylation of Isoserine Derivatives Followed by Nucleophilic Ring Opening of Quaternary Sulfamidates

    The Journal of Organic Chemistry, Vol. 87, Núm. 13, pp. 8730-8743

2020

  1. Synthesis of Nβ-Substituted α,β-Diamino Acids via Stereoselective N-Michael Additions to a Chiral Bicyclic Dehydroalanine

    Journal of Organic Chemistry, Vol. 85, Núm. 5, pp. 3134-3145

2018

  1. Cell-Penetrating Peptides Containing Fluorescent d-Cysteines

    Chemistry - A European Journal, Vol. 24, Núm. 31, pp. 7991-8000

  2. Oxygen by Carbon Replacement at the Glycosidic Linkage Modulates the Sugar Conformation in Tn Antigen Mimics

    ACS Omega, Vol. 3, Núm. 12, pp. 18142-18152

  3. Stereoselective S-Michael additions of sulphur nucleophiles to a chiral dehydroalanine. Synthesis of fluorescent peptides

    16th Iberian Peptide Meeting/4th ChemBio Group Meeting

2016

  1. Bifunctional Chiral Dehydroalanines for Peptide Coupling and Stereoselective S-Michael Addition

    Organic Letters, Vol. 18, Núm. 12, pp. 2796-2799

  2. Conformationally-locked C-glycosides: tuning aglycone interactions for optimal chaperone behaviour in Gaucher fibroblasts

    Organic and Biomolecular Chemistry, Vol. 14, Núm. 4, pp. 1473-1484

2014

  1. A double diastereoselective Michael-type addition as an entry to Tn antigen mimics and analogs of Thiamet-G

    XI Carbohydrate Symposium

2013

  1. A double diastereoselective michael-type addition as an entry to conformationally restricted Tn antigen mimics

    Journal of Organic Chemistry, Vol. 78, Núm. 21, pp. 10968-10977