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TEMPO-catalyzed oxidative homocoupling route to 3,2′-biindolin-2-ones via an indolin-3-one intermediate
| Content Provider | Semantic Scholar |
|---|---|
| Author | Huang, Panpan Lu, Yingbing Liu, Liangxian |
| Copyright Year | 2017 |
| Abstract | A combinative C2-selective arylation, and C3-selective carbonylation of free indole derivatives, by means of TEMPO catalysis and a silver oxidant under non-directing group conditions, was successful demonstrated. This new methodology is both atom and step efficient and is applicable to a broad scope of substrates, allowing the synthesis of a range of synthetically valuable 3,2′-biindolin-2-ones in moderate to excellent yields. |
| Starting Page | 606 |
| Ending Page | 610 |
| Page Count | 5 |
| File Format | PDF HTM / HTML |
| DOI | 10.1039/C6RA24834A |
| Alternate Webpage(s) | http://pubs.rsc.org/en/content/articlepdf/2017/ra/c6ra24834a |
| Alternate Webpage(s) | https://pubs.rsc.org/en/content/articlepdf/2017/ra/c6ra24834a |
| Alternate Webpage(s) | http://www.rsc.org/suppdata/c6/ra/c6ra24834a/c6ra24834a1.pdf |
| Alternate Webpage(s) | https://doi.org/10.1039/C6RA24834A |
| Volume Number | 7 |
| Language | English |
| Access Restriction | Open |
| Content Type | Text |
| Resource Type | Article |