Please use this identifier to cite or link to this item:
|Title:||Thiolate photocatalysis enables radical borylation of reductively inert aryl electrophiles||Authors:||Li, Haoyu
|Keywords:||Science::Chemistry||Issue Date:||2021||Source:||Li, H. & Chiba, S. (2021). Thiolate photocatalysis enables radical borylation of reductively inert aryl electrophiles. Chem, 7(6), 1414-1416. https://dx.doi.org/10.1016/j.chempr.2021.05.015||Journal:||Chem||Abstract:||The facile installation of functionalities to aromatic compounds via chemical activation of inert carbon-heteroatom bonds is a challenging task. In this issue of Chem, König and co-workers disclose a photocatalytic protocol for the radical borylation of reductively inert aryl electrophiles, such as aryl fluorides and aryl carbonates, by using simple thiolate salts as a catalyst.||URI:||https://hdl.handle.net/10356/157069||ISSN:||2451-9294||DOI:||10.1016/j.chempr.2021.05.015||Schools:||School of Physical and Mathematical Sciences||Rights:||© 2021 Elsevier Inc. All rights reserved.||Fulltext Permission:||none||Fulltext Availability:||No Fulltext|
|Appears in Collections:||SPMS Journal Articles|
Updated on Sep 26, 2023
Items in DR-NTU are protected by copyright, with all rights reserved, unless otherwise indicated.