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Asymmetric Copper-Catalyzed Azide–Alkyne Cycloadditions
| Content Provider | Semantic Scholar |
|---|---|
| Author | Brittain, William D. G. Buckley, Benjamin R. Fossey, John S. |
| Copyright Year | 2016 |
| Abstract | Since its discovery independently by Sharpless and Meldal in 2002, the copper-catalyzed azide–alkyne cycloaddition (CuAAC) has become a ubiquitous molecular linking platform. Easy access to substituted 1,4-triazoles can be exploited to engender asymmetry to a myriad of potentially useful targets in high yields. Utilizing the CuAAC to form chiral triazolic products in a single step is an attractive and powerful approach for the synthetic chemist. The area of asymmetric CuAAC is still in its infancy compared to more established asymmetric metal-mediated transformations; however, this leads to exciting challenges that need to be overcome to usher in the next era in the story of the triazole and click chemistry in general. This review details the steps taken into asymmetric CuAAC and the exciting results achieved thus far. |
| Starting Page | 3629 |
| Ending Page | 3636 |
| Page Count | 8 |
| File Format | PDF HTM / HTML |
| DOI | 10.1021/acscatal.6b00996 |
| Alternate Webpage(s) | https://core.ac.uk/download/pdf/42485693.pdf |
| Alternate Webpage(s) | https://dspace.lboro.ac.uk/dspace-jspui/bitstream/2134/21364/1/Asymmetric%20CuAAC%20ACS.pdf |
| Alternate Webpage(s) | http://wxjs.chinayyhg.com/upload/Files/20160629073959512/20160629074026153.pdf |
| Alternate Webpage(s) | https://doi.org/10.1021/acscatal.6b00996 |
| Volume Number | 6 |
| Language | English |
| Access Restriction | Open |
| Content Type | Text |
| Resource Type | Article |
