This review focuses on synthetic strategies developed to obtain serine-proline chimeras. The conformational properties of proline, combined with functional groups typical of aminoacid side chains, represent an interesting approach to stabilize peptide secondary structures such as -turns. Different chemical pathways to synthesize 3-, 4-, and 5-hydroxyprolines, considered proline chimeras of aminoacid serine, will be presented and discussed.

Synthetic Strategies to Serine-Proline Chimeras: An Overview / Ammazzalorso, Alessandra; Filippis, Barbara; Maccallini, Cristina; Pierini, Marco. - In: CURRENT BIOACTIVE COMPOUNDS. - ISSN 1573-4072. - STAMPA. - 12:3(2016), pp. 136-145. [10.2174/1573407212666160511150017]

Synthetic Strategies to Serine-Proline Chimeras: An Overview

PIERINI, MARCO
2016

Abstract

This review focuses on synthetic strategies developed to obtain serine-proline chimeras. The conformational properties of proline, combined with functional groups typical of aminoacid side chains, represent an interesting approach to stabilize peptide secondary structures such as -turns. Different chemical pathways to synthesize 3-, 4-, and 5-hydroxyprolines, considered proline chimeras of aminoacid serine, will be presented and discussed.
2016
Aminoacid, homoserine, hydroxyprolines, proline chimeras, serine, synthesis.
01 Pubblicazione su rivista::01a Articolo in rivista
Synthetic Strategies to Serine-Proline Chimeras: An Overview / Ammazzalorso, Alessandra; Filippis, Barbara; Maccallini, Cristina; Pierini, Marco. - In: CURRENT BIOACTIVE COMPOUNDS. - ISSN 1573-4072. - STAMPA. - 12:3(2016), pp. 136-145. [10.2174/1573407212666160511150017]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/894546
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