2,3-Diaminopropanols Obtained from d-Serine as Intermediates in the Synthesis of Protected 2,3-l-Diaminopropanoic Acid (l-Dap) Methyl Esters

A synthetic strategy for the preparation of two orthogonally protected methyl esters of the non-proteinogenic amino acid 2,3-l-diaminopropanoic acid (l-Dap) was developed. In these structures, the base-labile protecting group 9-fluorenylmethyloxycarbonyl (Fmoc) was paired to the p-toluensulfonyl (to...

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Detalles Bibliográficos
Autores principales: Temperini, Andrea, Aiello, Donatella, Mazzotti, Fabio, Athanassopoulos, Constantinos M., De Luca, Pierantonio, Siciliano, Carlo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7145313/
https://www.ncbi.nlm.nih.gov/pubmed/32183079
http://dx.doi.org/10.3390/molecules25061313

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7145313/
https://www.ncbi.nlm.nih.gov/pubmed/32183079
http://dx.doi.org/10.3390/molecules25061313

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