Department of Chemistry, School of Science, The University of Tokyo, Hongo, Bunkyo-ku, Tokyo, 113-0033, Japan.
Angew Chem Int Ed Engl. 2021 Jun 1;60(23):12786-12790. doi: 10.1002/anie.202102506. Epub 2021 May 1.
Development of stable heterogeneous catalyst systems is a crucial subject to achieve sustainable society. Though metal nanoparticles are robust species, the study of asymmetric catalysis by them has been restricted because methods to activate metal nanoparticles without causing metal leaching were limited. We developed Rh nanoparticle catalysts (NCI-Rh) supported on nitrogen-doped carbon as a solid ligand to interact with metals for asymmetric insertion of carbenoids into N-H bonds cocatalyzed by chiral phosphoric acid. Nitrogen dopants played a crucial role in both catalytic activity and enantioselectivity while almost no catalysis was observed with Rh nanoparticles immobilized on supports without nitrogen dopants. Various types of chiral α-amino acid derivatives were synthesized in high yields with high enantioselectivities and NCI-Rh could be reused in seven runs. Furthermore, we demonstrated the corresponding continuous-flow reaction using a column packed with NCI-Rh. The desired product was obtained efficiently for over 90 h through the reactivation of NCI-Rh and the chiral source could be recovered.
发展稳定的多相催化剂体系是实现可持续社会的关键课题。尽管金属纳米粒子是稳定的物种,但由于缺乏激活金属纳米粒子而不导致金属浸出的方法,它们在不对称催化中的研究受到限制。我们开发了负载在氮掺杂碳上的 Rh 纳米粒子催化剂(NCI-Rh)作为一种固体配体,与金属相互作用,在手性磷酸的共催化下,将碳烯类化合物不对称地插入 N-H 键中。氮掺杂剂在催化活性和对映选择性方面都起着至关重要的作用,而固定在没有氮掺杂剂的载体上的 Rh 纳米粒子几乎没有催化作用。各种类型的手性α-氨基酸衍生物以高产率和高对映选择性合成,NCI-Rh 可以重复使用七次。此外,我们使用填充有 NCI-Rh 的柱进行了相应的连续流动反应。通过 NCI-Rh 的再活化,可以有效地获得所需产物超过 90 小时,并且可以回收手性源。