Acyl hydrazides as peptoid sub-monomers

Literature Information

Publication Date 2011-09-05
DOI 10.1039/C1CC12750K
Impact Factor 6.222
Authors

Bani Kanta Sarma, Muhammed Yousufuddin, Thomas Kodadek


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Abstract

The use of acyl hydrazides as peptoid sub-monomers is investigated. We demonstrate here that azapeptoids derived entirely from acyl hydrazides can be made conveniently and efficiently using standard peptoid sub-monomer chemistry. Structural studies reveal that the main chain amide bond in these molecules predominantly adopts a trans conformation. A high-quality one bead one compound library of tetramers was made by split and pool synthesis and we found that the identity of the molecule on a single bead could be determined by tandem MALDI mass spectrometry.

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