| Literature DB >> 33986970 |
Jianyu Xu1, Olivia P Bercher1, Michael R Talley1, Mary P Watson1.
Abstract
Highly enantioenriched benzylic and allylic amines and alcohols are readily available via asymmetric synthesis and in complex natural products. The development of mild, nickel-catalyzed cross-couplings of their derivatives has advanced the tools available for the preparation of a range of highly enantioenriched products, including those with quaternary stereocenters. This perspective focuses on cross-couplings with convenient and functional group-tolerant organoboron reagents and highlights the discoveries of activating groups and conditions that have led to high-yielding and highly stereospecific reactions. Emphasis is placed on mechanistic understanding, particularly with regards to controlling inversion vs. retention pathways. Limitations and opportunities for future developments are also highlighted.Entities:
Keywords: Alcohols; Amines; Cross-couplings; Nickel Catalysis; Organoboron; Stereospecific
Year: 2021 PMID: 33986970 PMCID: PMC8112725 DOI: 10.1021/acscatal.0c05484
Source DB: PubMed Journal: ACS Catal Impact factor: 13.084