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- W4230508082 abstract "A fast, new route to peptide thioesters is presented, using selenocysteine at the C-terminus of peptides prepared from solid-phase peptide synthesis. Thioester formation is initiated via an N→Se acyl shift and can occur at lower temperatures and in shorter time scales than previously seen when using cysteine in this way. This strategy also has been shown to accelerate the cyclization of an antimicrobial peptide." @default.
- W4230508082 created "2022-05-11" @default.
- W4230508082 date "2013-02-01" @default.
- W4230508082 modified "2023-09-27" @default.
- W4230508082 doi "https://doi.org/10.1002/psc.v19.2" @default.
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