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.
我们研究了酰
肼作为肽类次单体的用途。我们在此证明,完全由酰基酰
肼衍生的氮杂
环庚烷可以通过标准的
庚烷亚单体
化学反应方便、高效地制造出来。结构研究表明,这些分子中的主链酰胺键主要采用反式构象。我们发现,单个珠子上分子的身份可以通过串联 MALDI 质谱来确定。