Dual Ni/photoredox-catalyzed asymmetric cross-coupling to access chiral benzylic boronic esters
Purui Zheng,
Pan Zhou,
Dong Wang,
Wenhao Xu,
Hepan Wang and
Tao Xu ()
Additional contact information
Purui Zheng: Tongji University
Pan Zhou: Tongji University
Dong Wang: Tongji University
Wenhao Xu: Tongji University
Hepan Wang: Tongji University
Tao Xu: Tongji University
Nature Communications, 2021, vol. 12, issue 1, 1-9
Abstract:
Abstract The flourishing Ni/photoredox-catalyzed asymmetric couplings typically rely on redox-neutral reactions. In this work, we report a reductive cross-coupling of aryl iodides and α-chloroboranes under a dual catalytic regime to further enrich the metallaphotoredox chemistry. This approach proceeds under mild conditions (visible light, ambient temperature, no strong base) to access the versatile benzylic boronic esters with good functional group tolerance and excellent enantioselectivities.
Date: 2021
References: Add references at CitEc
Citations:
Downloads: (external link)
https://www.nature.com/articles/s41467-021-21947-1 Abstract (text/html)
Related works:
This item may be available elsewhere in EconPapers: Search for items with the same title.
Export reference: BibTeX
RIS (EndNote, ProCite, RefMan)
HTML/Text
Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-21947-1
Ordering information: This journal article can be ordered from
https://www.nature.com/ncomms/
DOI: 10.1038/s41467-021-21947-1
Access Statistics for this article
Nature Communications is currently edited by Nathalie Le Bot, Enda Bergin and Fiona Gillespie
More articles in Nature Communications from Nature
Bibliographic data for series maintained by Sonal Shukla () and Springer Nature Abstracting and Indexing ().