Please use this identifier to cite or link to this item:
http://hdl.handle.net/10397/100118
| DC Field | Value | Language |
|---|---|---|
| dc.contributor | Department of Applied Biology and Chemical Technology | en_US |
| dc.creator | Chan, CM | en_US |
| dc.creator | Chow, YC | en_US |
| dc.creator | Yu, WY | en_US |
| dc.date.accessioned | 2023-08-08T01:52:18Z | - |
| dc.date.available | 2023-08-08T01:52:18Z | - |
| dc.identifier.issn | 0039-7881 | en_US |
| dc.identifier.uri | http://hdl.handle.net/10397/100118 | - |
| dc.language.iso | en | en_US |
| dc.publisher | Georg Thieme Verlag | en_US |
| dc.rights | © Georg Thieme Verlag Stuttgart · New York | en_US |
| dc.rights | This is the accepted version of the following article: Chan, C. M., Chow, Y. C., & Yu, W. Y. (2020). Recent Advances in Photocatalytic C–N Bond Coupling Reactions. Synthesis, 52(20), 2899-2921, which has been published in https://doi.org/10.1055/s-0040-1707136. | en_US |
| dc.subject | Amination | en_US |
| dc.subject | C-N cross-coupling | en_US |
| dc.subject | Photochemistry | en_US |
| dc.subject | Radicals | en_US |
| dc.subject | Visible light | en_US |
| dc.title | Recent advances in photocatalytic C–N bond coupling reactions | en_US |
| dc.type | Journal/Magazine Article | en_US |
| dc.identifier.spage | 2899 | en_US |
| dc.identifier.epage | 2921 | en_US |
| dc.identifier.volume | 52 | en_US |
| dc.identifier.issue | 20 | en_US |
| dc.identifier.doi | 10.1055/s-0040-1707136 | en_US |
| dcterms.abstract | Catalytic C-N bond formation is one of the major research topics in synthetic chemistry owing to the ubiquity of amino groups in natural products, synthetic intermediates and pharmaceutical agents. In parallel with well-established metal-catalyzed C-N bond coupling protocols, photocatalytic reactions have recently emerged as efficient and selective alternatives for the construction of C-N bonds. In this review, the progress made on photocatalytic C-N bond coupling reactions between 2012 and February 2020 is summarized. | en_US |
| dcterms.abstract | 1 Introduction | en_US |
| dcterms.abstract | 1.1 General Mechanisms for Photoredox Catalysis | en_US |
| dcterms.abstract | 1.2 Pioneering Work | en_US |
| dcterms.abstract | 2 C(sp 2)-N Bond Formation | en_US |
| dcterms.abstract | 2.1 Protocols Involving an External Oxidant | en_US |
| dcterms.abstract | 2.2 Oxidant-Free Protocols | en_US |
| dcterms.abstract | 3 C(sp 3)-N Bond Formation | en_US |
| dcterms.abstract | 3.1 Direct Radical-Radical Coupling | en_US |
| dcterms.abstract | 3.2 Addition Reactions to Alkenes | en_US |
| dcterms.abstract | 3.3 Reductive Amination of Carbonyl Compounds | en_US |
| dcterms.abstract | 3.4 Decarboxylative Amination | en_US |
| dcterms.abstract | 4 Cyclization Reactions | en_US |
| dcterms.abstract | 4.1 C(sp 2)-N Heterocycle Formation | en_US |
| dcterms.abstract | 4.2 C(sp 3)-N Heterocycle Formation | en_US |
| dcterms.abstract | 5 Other Examples 6 | en_US |
| dcterms.abstract | Conclusion and Outlook | en_US |
| dcterms.accessRights | open access | en_US |
| dcterms.bibliographicCitation | Synthesis, Oct. 2020, v. 52, no. 20, p. 2899-2921 | en_US |
| dcterms.isPartOf | Synthesis | en_US |
| dcterms.issued | 2020-10 | - |
| dc.identifier.scopus | 2-s2.0-85092513657 | - |
| dc.description.validate | 202308 bckw | en_US |
| dc.description.oa | Accepted Manuscript | en_US |
| dc.identifier.FolderNumber | ABCT-0194 | - |
| dc.description.pubStatus | Published | en_US |
| dc.identifier.OPUS | 50632182 | - |
| dc.description.oaCategory | Green (AAM) | en_US |
| Appears in Collections: | Journal/Magazine Article | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| Chan_Recent_Advances_Photocatalytic.pdf | Pre-Published version | 1.46 MB | Adobe PDF | View/Open |
Page views
80
Citations as of Apr 14, 2025
Downloads
288
Citations as of Apr 14, 2025
SCOPUSTM
Citations
37
Citations as of Sep 12, 2025
WEB OF SCIENCETM
Citations
33
Citations as of Oct 10, 2024
Google ScholarTM
Check
Altmetric
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.



