Site-selective solid phase synthesis of carbonylated peptides

The aim of our research was to design an efficient method for the solid phase synthesis of carbonylated peptides. For this purpose, we designed and synthesized a fully protected derivative Fmoc-amino(2,5,5-trimetyhyl-1,3-dioxolan-2-yl)acetic acid (Fmoc-Atda-OH) of a novel unnatural amino acid (Thr(O...

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Detalles Bibliográficos
Autores principales: Waliczek, Mateusz, Kijewska, Monika, Stefanowicz, Piotr, Szewczuk, Zbigniew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Vienna 2015
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4458268/
https://www.ncbi.nlm.nih.gov/pubmed/25813939
http://dx.doi.org/10.1007/s00726-015-1967-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4458268/
https://www.ncbi.nlm.nih.gov/pubmed/25813939
http://dx.doi.org/10.1007/s00726-015-1967-4

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