Preparation of modified peptides: direct conversion of α-amino acids into β-amino aldehydes.
Carlos J Saavedra, Alicia Boto, Rosendo Hernández
Index: Org. Biomol. Chem. 10(22) , 4448-61, (2012)
Full Text: HTML
Abstract
A direct method for the transformation of α-amino acids into β-amino aldehydes was developed, and applied to the modification of the C-terminal residue of peptides. The method takes place in good yields and under mild conditions. The application of this methodology to the preparation of small peptides with γ-amino alcohol units, which are precursors of analogues of peptaibol antibiotics, is also described.
Related Compounds
Related Articles:
Induction of the SOS function sfiA in E. coli by systems which generate triplet ketones.
1988-03-01
[Mutat. Res. 198(1) , 53-60, (1988)]
1993-04-01
[Toxicol. Lett. 67(1-3) , 17-28, (1993)]