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- W2497816615 abstract "Recently, a novel type of antimicrobial and proteolytically stable peptidomimetic oligomers having an α-peptide-β-peptoid chimeric backbone was reported. The present paper describes efficient protocols for the preparation of a wide range of dimeric building blocks, displaying different types of side-chains, for use in solid-phase synthesis (SPS) of libraries of this type of oligomers. The β-peptoid monomers were obtained by microwave-assisted aza-Michael additions to acrylic esters. Subsequent solution-phase peptide coupling with suitably protected α-amino acids afforded dimeric intermediates. Even sluggish peptide couplings, involving sterically hindered N-alkyl-β-alanines or amino acids with bulky side-chains, gave high yields on multigram-scale when using microwave (MW) irradiation. Protecting group and side-chain manipulations were performed as one-pot solution-phase procedures to afford ten different building blocks in good to excellent yields. Finally, the efficiency of SPS oligomerization of a representative dimer was demonstrated by preparing 10- to 16-residue homomers and by the assembly of four different building blocks to give a diversely functionalized octamer." @default.
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- W2497816615 date "2008-07-08" @default.
- W2497816615 modified "2023-10-18" @default.
- W2497816615 title "Dimeric Building Blocks for Solid-Phase Synthesis of α-Peptide-β-Peptoid Chimeras" @default.
- W2497816615 doi "https://doi.org/10.1055/s-2008-1067171" @default.
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