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Asymmetric synthesis of cyclopentanones through dual Lewis acid-catalysed [3+2]-cycloaddition of donor-acceptor cyclopropanes with ketenes.
| Content Provider | Semantic Scholar |
|---|---|
| Author | Mondal, Mukulesh Panda, Manashi Davis, Nicholas W. McKee, Vickie Kerrigan, Nessan J. |
| Copyright Year | 2019 |
| Abstract | When InBr3-EtAlCl2 (15-30 mol%) was used as a dual Lewis acid system to promote the formal [3+2]-cycloaddition of enantioenriched donor-acceptor cyclopropanes with ketenes, cyclopentanones were formed in good to excellent yields (84-99%, 18 examples), and with excellent transfer of chirality (15 examples, 90% ee to >99% ee). |
| File Format | PDF HTM / HTML |
| DOI | 10.1039/c9cc07477e |
| Alternate Webpage(s) | http://www.rsc.org/suppdata/c9/cc/c9cc07477e/c9cc07477e2.pdf |
| PubMed reference number | 31650999 |
| Alternate Webpage(s) | https://doi.org/10.1039/c9cc07477e |
| Journal | Medline |
| Journal | Chemical communications |
| Language | English |
| Access Restriction | Open |
| Content Type | Text |
| Resource Type | Article |