Please use this identifier to cite or link to this item:
http://localhost:8080/xmlui/handle/123456789/3213
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Ani, Deepthi | - |
dc.contributor.author | Vidya, Sathi | - |
dc.contributor.author | Vijay, Nair | - |
dc.date.accessioned | 2018-07-26T06:19:02Z | - |
dc.date.available | 2018-07-26T06:19:02Z | - |
dc.date.issued | 2018-07-18 | - |
dc.identifier.citation | Tetrahedron Letters, 59(29):2767-2777 | en_US |
dc.identifier.uri | http://10.10.100.66:8080/xmlui/handle/123456789/3213 | - |
dc.description.abstract | Radical reactions have been a fascinating arena in organic chemistry for decades and the rapid progress in this field is the topic of this review. Generation of radicals through sustainable catalysis using photoredox catalysts and iron based catalysts have significantly expanded the scope of radical reactions for carbon–carbon and carbon-heteroatom bond formations in recent years. Selective transformations using silver salts and other single electron transfer oxidants have also played significant roles. Cascade reactions based on radical intermediates have even widened the potential of radical reactions for carbocyclic and heterocyclic constructions. The recent advances (2014–2017) in radical based methods for CAC bond formations are discussed in this digest review. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Elsevier | en_US |
dc.subject | Sustainable catalysis | en_US |
dc.subject | C-C bond formation | en_US |
dc.subject | Photoredox catalysis | en_US |
dc.subject | Single electron transfer | en_US |
dc.subject | Radical cascade | en_US |
dc.title | Recent topics of radical-based carbon-carbon bond formations | en_US |
dc.type | Article | en_US |
Appears in Collections: | 2018 |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
Recent topics of radical-Ani Deepthi-Tetrahedron Letters.pdf Restricted Access | 1.87 MB | Adobe PDF | View/Open Request a copy |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.