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Copper-catalyzed enantioselective Mukaiyama aldol reaction of silyl enol ethers with isatins.
| Content Provider | Semantic Scholar |
|---|---|
| Author | Li, Jindong Li, Yan-An Sun, Jianan Gui, Yang Huang, Yekai Zha, Zhenggen Wang, Zhiyong |
| Copyright Year | 2019 |
| Abstract | A highly enantioselective Mukaiyama aldol reaction of silyl enol ethers with isatins catalyzed by chiral copper complexes was developed. A series of chiral 3-substituted 3-hydroxy-2-oxindoles bearing a tetra-substituted center could be obtained exclusively with high yields (up to 95%) and excellent enantioselectivities (up to 99%). In particular, water was essential to improve the diastereoselectivity. |
| Starting Page | 6309 |
| Ending Page | 6312 |
| Page Count | 4 |
| File Format | PDF HTM / HTML |
| DOI | 10.1039/c9cc02159k |
| PubMed reference number | 31089588 |
| Journal | Medline |
| Volume Number | 55 |
| Issue Number | 44 |
| Alternate Webpage(s) | http://www.rsc.org/suppdata/c9/cc/c9cc02159k/c9cc02159k1.pdf |
| Alternate Webpage(s) | https://doi.org/10.1039/c9cc02159k |
| Journal | Chemical communications |
| Language | English |
| Access Restriction | Open |
| Content Type | Text |
| Resource Type | Article |