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Non-natural 3-Arylmorpholino-β-amino Acid as a PPII Helix Inducer

[Image: see text] A new non-natural β-amino acid, named 3-Ar-β-Morph, was designed and synthesized via a regio- and diastereoselective Pd-catalyzed C(sp(3))H-arylation of the corresponding 2S,6S-(6-methoxymorpholin-2-yl)carboxylic acid, readily available from glucose. According to the computational...

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Detalles Bibliográficos
Autores principales: Vaghi, Francesco, Bucci, Raffaella, Clerici, Francesca, Contini, Alessandro, Gelmi, M. Luisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8009597/
https://www.ncbi.nlm.nih.gov/pubmed/32790435
http://dx.doi.org/10.1021/acs.orglett.0c02331
Descripción
Sumario:[Image: see text] A new non-natural β-amino acid, named 3-Ar-β-Morph, was designed and synthesized via a regio- and diastereoselective Pd-catalyzed C(sp(3))H-arylation of the corresponding 2S,6S-(6-methoxymorpholin-2-yl)carboxylic acid, readily available from glucose. According to the computational prevision and confirmed by IR and NMR data, the insertion of 3-Ar-β-Morph in a model foldamer represents a way to stabilize a PPII-like helix through the presence of two γ-turns, secondary structure motifs induced by the morpholine ring, and the trans-tertiary amide bond.