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DOI: 10.1055/s-0041-1737549
Solid-Phase Synthesis of α-Amino Alkyl or Aryl Phosphonopeptide Derivatives
An Expedient Method for the Solid-Phase Synthesis of α-Aminoalkyl Phosphonopeptides.
Tetrahedron Lett. 2002;
43: 4103-4106
DOI: 10.1016/S0040-4039(02)00695-0

Significance
Amino phosphonopeptides are highly significant molecules in biological systems as potent antimicrobial agents and as inhibitors of various enzymes. In 2002, Houghten and co-workers developed a solid-phase synthesis of α-aminoalkyl phosphonopeptides by using an aldehyde dimethylphosphite in the presence of the Lewis acid BF3·Et2O.
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Comment
The developed method is one of the simplest and practically most viable methods for the generation of series of α-aminoalkyl or aryl phosphonopeptide derivatives in high yields with moderate stereoselectivity. The method can be used for the synthesis of libraries of peptide or nonpeptide phosphonates.
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Publication History
Article published online:
18 March 2022
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