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Fernando Albericio

Researcher at University of KwaZulu-Natal

Publications -  1012
Citations -  29912

Fernando Albericio is an academic researcher from University of KwaZulu-Natal. The author has contributed to research in topics: Peptide synthesis & Solid-phase synthesis. The author has an hindex of 76, co-authored 965 publications receiving 26146 citations. Previous affiliations of Fernando Albericio include University of Barcelona & University of Chile.

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S-2-(2,4-dinitrophenyl)ethyl-L-cysteine: a new derivative for solid-phase peptide synthesis

TL;DR: The S-2-(2,4-dinitrophenyl)ethyl-L-cysteine derivative is fully compatible with the Boc/Bzl solid phase peptide synyhesis strategy and can be smoothly and quantitatively removed to give the free thiol or a disulfide bridge.
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Synthesis of Fmoc-protected amino ketones bearing tert-butyl based side-chain protecting groups

TL;DR: A variety of Fmoc-protected amino ketones have been prepared in good yields from amino acids by their transformation into thioesters of 2-mercaptopyridine and reaction of the resulting products with dialkylcuprates as mentioned in this paper.
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One pot synthesis, molecular structure and spectroscopic studies (X-ray, IR, NMR, UV-Vis) of novel 2-(4,6-dimethoxy-1,3,5-triazin-2-yl) amino acid ester derivatives.

TL;DR: The B3LYP/6-311G(d,p) calculated molecular structures are well correlated with the geometrical parameters obtained from the X-ray analyses and the spectroscopic properties such as IR vibrational modes, NMR chemical shifts and UV-Vis electronic transitions were discussed both experimentally and theoretically.
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A simple protocol for combinatorial cyclic depsipeptide libraries sequencing by matrix-assisted laser desorption/ionisation mass spectrometry.

TL;DR: A simple protocol for combinatorial cyclic libraries synthesis and ring opening before MS analysis is proposed, suitable for the preparation of one‐bead‐one‐cyclic depsipeptide libraries that can be easily open for its sequencing by matrix‐assisted laser desorption/ionisation MS.