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- W2011787057 abstract "Five protected submonomers for peptoid synthesis were prepared, including Nin-BOC-tryptamine, O-t-butyl tyramine, PMC-guanidino-propylamine, 6-amino-6-deoxy-d-galactopyranose diacetonide, and 5-amino-2,2-dimethyl-1,3-dioxane. The first three mimic natural aminoacid sidechains i.e. tryptophan, tyrosine, and arginine, while the last two provide hydrophilic sidechains. These submonomers were successfully used for preparation of oligo-peptoids by the submonomer synthesis method." @default.
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- W2011787057 date "1999-02-01" @default.
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- W2011787057 title "New submonomers for poly N-substituted glycines (peptoids)" @default.
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- W2011787057 doi "https://doi.org/10.1016/s0040-4039(98)02696-3" @default.
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