Department of Chemistry, Colorado School of Mines, 1500 Illinois St., Golden, CO 80401, USA.
Quantitative Biology and Engineering Program, Colorado School of Mines, 1500 Illinois St., Golden, CO 80401, USA.
Chemistry. 2024 Feb 1;30(7):e202302485. doi: 10.1002/chem.202302485. Epub 2023 Dec 15.
Iminoboronates and diazaborines are related classes of compounds that feature an imine ortho to an arylboronic acid (iminoboronate) or a hydrazone that cyclizes with an ortho arylboronic acid (diazaborine). Rather than acting as independent chemical motifs, the arylboronic acid impacts the rate of imine/hydrazone formation, hydrolysis, and exchange with competing nucleophiles. Increasing evidence has shown that the imine/hydrazone functionality also impacts arylboronic acid reactivity toward diols and reactive oxygen and nitrogen species (ROS/RNS). Untangling the communication between C=N linked functionalities and arylboronic acids has revealed a powerful and tunable motif for bioconjugation chemistries and other applications in chemical biology. Here, we survey the applications of iminoboronates and diazaborines in these fields with an eye toward understanding their utility as a function of neighboring group effects.
亚氨基硼酸酯和重氮硼烷是两类相关的化合物,它们的特点是亚胺位于芳基硼酸(亚氨基硼酸酯)或腙的邻位,与邻位芳基硼酸环化(重氮硼烷)。芳基硼酸不仅作为独立的化学基序发挥作用,还会影响亚胺/腙的形成、水解和与竞争亲核试剂的交换速率。越来越多的证据表明,亚胺/腙的官能团也会影响芳基硼酸与二醇和活性氧和氮物种(ROS/RNS)的反应性。阐明 C=N 连接官能团和芳基硼酸之间的通讯,揭示了用于生物缀合化学和化学生物学中其他应用的强大且可调谐的基序。在这里,我们调查了亚氨基硼酸酯和重氮硼烷在这些领域的应用,着眼于了解它们作为邻基效应函数的实用性。