2,3-Diaminopropanols Obtained from <span style="font-variant: small-caps">d</span>-Serine as Intermediates in the Synthesis of Protected 2,3-<span style="font-variant: small-caps">l</span>-Diaminopropanoic Acid (<span style="font-variant: small-caps">l</span>-Dap) Methyl Esters

2,3-Diaminopropanols Obtained from <span style="font-variant: small-caps">d</span>-Serine as Intermediates in the Synthesis of Protected 2,3-<span style="font-variant: small-caps">l</span>-Diaminopropanoic Acid (<span style="font-variant: small-caps">l</span>-Dap) Methyl Esters

A synthetic strategy for the preparation of two orthogonally protected methyl esters of the non-proteinogenic amino acid 2,3-<span style="font-variant: small-caps;">l</span>-diaminopropanoic acid<span style="font-variant: small-caps;"> (l</span>-Dap) was d...

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Bibliographic Details
Main Authors:	Andrea Temperini, Donatella Aiello, Fabio Mazzotti, Constantinos M. Athanassopoulos, Pierantonio De Luca, Carlo Siciliano
Format:	Article
Language:	English
Published:	MDPI AG 2020-03-01
Series:	Molecules
Subjects:	2,3-<span style="font-variant: small-caps">l</span>-diaminopropanoic acid <span style="font-variant: small-caps">l</span>-dap basic amino acids serine reductive amination orthogonal protecting groups 1,3,5-trichloro-2,4,6-triazinetrione trichloroisocyanuric acid (tcca) (2,2,6,6-tetramethylpiperidi-1-yl)oxyl (tempo) <i>n</i>-methylation
Online Access:	https://www.mdpi.com/1420-3049/25/6/1313

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