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手性池跳跃:早期金属的手性氢胺化反应。

Jumping in the Chiral Pool: Asymmetric Hydroaminations with Early Metals.

机构信息

TU Chemnitz, Research Center for Materials, Architectures and Integration of Nanomembranes (MAIN), Research Group Organometallic Chemistry, Rosenbergstraße 6, D-09126 Chemnitz, Germany.

出版信息

Molecules. 2023 Mar 16;28(6):2702. doi: 10.3390/molecules28062702.

Abstract

The application of early-metal-based catalysts featuring natural chiral pool motifs, such as amino acids, terpenes and alkaloids, in hydroamination reactions is discussed and compared to those beyond the chiral pool. In particular, alkaline (Li), alkaline earth (Mg, Ca), rare earth (Y, La, Nd, Sm, Lu), group IV (Ti, Zr, Hf) metal-, and tantalum-based catalytic systems are described, which in recent years improved considerably and have become more practical in their usability. Additional emphasis is directed towards their catalytic performance including yields and regio- as well as stereoselectivity in comparison with the group IV and V transition metals and more widely used rare earth metal-based catalysts.

摘要

本文讨论了在氨化反应中应用天然手性池分子(如氨基酸、萜类和生物碱)作为早期金属基催化剂,并将其与手性池以外的催化剂进行了比较。特别是,本文描述了碱性(Li)、碱土金属(Mg、Ca)、稀土金属(Y、La、Nd、Sm、Lu)、第 IV 族(Ti、Zr、Hf)金属以及钽基催化体系,近年来这些体系得到了极大的改善,在可用性方面变得更加实用。本文还特别强调了它们的催化性能,包括与第 IV 族和第 V 族过渡金属以及更广泛使用的基于稀土金属的催化剂相比的产率、区域和立体选择性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfe3/10058505/676d87f38e80/molecules-28-02702-sch002.jpg

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