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Updated: Sep 5, 2025

Modification and Functionalization of the Guanidine Group by Tailor-made Precursors
Published on: April 27, 2017
Deoxyfluorinating reagents as tools for γ-amino-α-hydroxyphosphonate modification
Marcin Kaźmierczak1,2, Grzegorz Dutkiewicz1, Henryk Koroniak1
1Faculty of Chemistry, Adam Mickiewicz University in Poznań, Uniwersytetu Poznańskiego 8, 61-614 Poznań, Poland. marcin.kazmierczak@amu.edu.pl.
Abstract:
Herein, we would like to present deoxyfluorinating reagents such as DAST and PyFluor and their successful use as tools for selective modification of γ-amino-α-hydroxyphosphonates. Depending on the deoxyfluorinating reagent applied, an intramolecular cyclization leading to phosphonates containing the 1,3-oxazinan-2-one moiety or direct nucleophilic deoxyfluorination yielding the α-fluorinated derivatives of γ-aminophosphonates was observed. The obtained compounds may be used as precursors in the preparation of medicinally important compounds e.g., dipeptide analogues or scaffolds containing the 1,3-oxazinan-2-one group.

