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https://hdl.handle.net/10356/157069| Title: | Thiolate photocatalysis enables radical borylation of reductively inert aryl electrophiles | Authors: | Li, Haoyu Chiba, Shunsuke |
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 |
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