Nickel-Catalyzed, Stereospecific C-C and C-B Cross-Couplings via C-N and C-O Bond Activation.

ACS Catal

Department of Chemistry & Biochemistry, University of Delaware, Newark, Delaware 19716, United States.

Published: February 2021

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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8112725PMC
http://dx.doi.org/10.1021/acscatal.0c05484DOI Listing

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