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Ricardo Riguera

Researcher at University of Santiago de Compostela

Publications -  270
Citations -  10544

Ricardo Riguera is an academic researcher from University of Santiago de Compostela. The author has contributed to research in topics: Absolute configuration & Proton NMR. The author has an hindex of 49, co-authored 269 publications receiving 9495 citations. Previous affiliations of Ricardo Riguera include Russian Academy of Sciences & University of Santiago, Chile.

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The assignment of absolute configuration by NMR

TL;DR: In this paper, the application of (S)-1,10-binaphthyl-2,20-diol as NMR chiral solvating agent (CSA) for omeprazole, and three of its analogs (lanso-, panto-, and rabe-prazole) was investigated.
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Development and brain delivery of chitosan-PEG nanoparticles functionalized with the monoclonal antibody OX26.

TL;DR: Findings indicate that this novel targeted nanoparticulate drug delivery system was able to translocate into the brain tissue after iv administration, and these novel nanoparticles are promising carriers for the transport of the anticaspase peptide Z-DEVD-FMK into thebrain.
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Reliable and Efficient Procedures for the Conjugation of Biomolecules through Huisgen Azide–Alkyne Cycloadditions

TL;DR: Key aspects found in the development of the efficient and benign functionalization of biomacromolecules through CuAAC, as well as the Cu-free strain-promoted azide-alkyne cycloaddition (SPAAC) are discussed.
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A practical guide for the assignment of the absolute configuration of alcohols, amines and carboxylic acids by NMR

TL;DR: A practical guide for the assignment of the absolute configuration of alcohols, amines and carboxylic acids by NMR is presented in this article, which includes information required for the judicious selection of the most suitable auxiliary reagent (MPA, MTPA, BPG, 9-AMA and 9-AHA), derivatization procedures and NMR conditions for each substrate, as well as a critical account on the reliability, scope and limitations of these applications.
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A Click Approach to Unprotected Glycodendrimers

TL;DR: Click chemistry in combination with ultrafiltration has allowed the quick, efficient, and reliable multivalent conjugation of unprotected alkyne-derived carbohydrates to three generations of azido-terminated gallic acid−triethylene glycol dendrimers under aqueous conditions.