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- W2000792513 abstract "Peptidomimetic compounds are increasingly important in drug-discovery applications. We introduce the synthesis of an N-substituted glycine oligomer, a bioactive “peptoid” trimer. The six-step protocol is conducted on solid-phase resin, enabling the synthesis to be performed by undergraduate organic chemistry students. This synthesis lab was successfully completed within one 4-h session by second-year students. The procedures are relatively inexpensive and versatile, enabling modifications to generate a variety of oligomer sequences from commercially available reagents including bromoacetic acid and a diverse set of primary amines." @default.
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- W2000792513 date "2010-05-11" @default.
- W2000792513 modified "2023-10-16" @default.
- W2000792513 title "Rapid Multistep Synthesis of a Bioactive Peptidomimetic Oligomer for the Undergraduate Laboratory" @default.
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- W2000792513 doi "https://doi.org/10.1021/ed100202f" @default.
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