Thiolate photocatalysis enables radical borylation of reductively inert aryl electrophiles
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...
Saved in:
| Main Authors: | , |
|---|---|
| Other Authors: | |
| Format: | Article |
| Language: | English |
| Published: |
2022
|
| Subjects: | |
| Online Access: | https://hdl.handle.net/10356/157069 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
| Institution: | Nanyang Technological University |
| Language: | English |
| id |
sg-ntu-dr.10356-157069 |
|---|---|
| record_format |
dspace |
| spelling |
sg-ntu-dr.10356-1570692022-05-02T06:32:18Z Thiolate photocatalysis enables radical borylation of reductively inert aryl electrophiles Li, Haoyu Chiba, Shunsuke School of Physical and Mathematical Sciences Science::Chemistry Photocatalysis Aryl Electrophiles 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. 2022-05-02T06:32:18Z 2022-05-02T06:32:18Z 2021 Journal Article 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 2451-9294 https://hdl.handle.net/10356/157069 10.1016/j.chempr.2021.05.015 2-s2.0-85107367072 6 7 1414 1416 en Chem © 2021 Elsevier Inc. All rights reserved. |
| institution |
Nanyang Technological University |
| building |
NTU Library |
| continent |
Asia |
| country |
Singapore Singapore |
| content_provider |
NTU Library |
| collection |
DR-NTU |
| language |
English |
| topic |
Science::Chemistry Photocatalysis Aryl Electrophiles |
| spellingShingle |
Science::Chemistry Photocatalysis Aryl Electrophiles Li, Haoyu Chiba, Shunsuke Thiolate photocatalysis enables radical borylation of reductively inert aryl electrophiles |
| description |
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. |
| author2 |
School of Physical and Mathematical Sciences |
| author_facet |
School of Physical and Mathematical Sciences Li, Haoyu Chiba, Shunsuke |
| format |
Article |
| author |
Li, Haoyu Chiba, Shunsuke |
| author_sort |
Li, Haoyu |
| title |
Thiolate photocatalysis enables radical borylation of reductively inert aryl electrophiles |
| title_short |
Thiolate photocatalysis enables radical borylation of reductively inert aryl electrophiles |
| title_full |
Thiolate photocatalysis enables radical borylation of reductively inert aryl electrophiles |
| title_fullStr |
Thiolate photocatalysis enables radical borylation of reductively inert aryl electrophiles |
| title_full_unstemmed |
Thiolate photocatalysis enables radical borylation of reductively inert aryl electrophiles |
| title_sort |
thiolate photocatalysis enables radical borylation of reductively inert aryl electrophiles |
| publishDate |
2022 |
| url |
https://hdl.handle.net/10356/157069 |
| _version_ |
1734310176766296064 |