Bose Ishani, Zhao Yan
Department of Chemistry, Iowa State University, Ames, Iowa 50011-3111, United States.
ACS Catal. 2020 Dec 4;10(23):13973-13977. doi: 10.1021/acscatal.0c03468. Epub 2020 Nov 17.
Nature has a remarkable ability to perform selective transformation of complex biological mixtures into desired products using enzymatic catalysts. We report the preparation of nanoparticle catalysts through molecular imprinting within cross-linked micelles. These catalysts were highly selective for their targeted substrates and could selectively hydrolyze less reactive acetals over more reactive ones even under basic conditions. Their catalytic activity and selectivity were tunable through rational postmodification of the active site. These properties enabled the nanoparticle catalysts to produce the desired β-nitro alcohol from a four-component acetal mixture in a tandem deprotection/Henry reaction that required incompatible acidic and basic catalysts in the two steps.
自然界具有非凡的能力,能够利用酶催化剂将复杂的生物混合物选择性地转化为所需产物。我们报道了通过在交联胶束内进行分子印迹来制备纳米颗粒催化剂。这些催化剂对其目标底物具有高度选择性,即使在碱性条件下,也能选择性地水解活性较低的缩醛,而不是活性较高的缩醛。通过对活性位点进行合理的后修饰,可以调节它们的催化活性和选择性。这些特性使纳米颗粒催化剂能够在串联脱保护/亨利反应中,从四组分缩醛混合物中制备所需的β-硝基醇,而该反应在两个步骤中需要不相容的酸性和碱性催化剂。