Please use this identifier to cite or link to this item:
http://hdl.handle.net/123456789/3387Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Mishra, U.K. | - |
| dc.contributor.author | Patel, Kaushalendra | - |
| dc.contributor.author | Ramasastry, S.S.V. | - |
| dc.date.accessioned | 2020-12-26T09:26:15Z | - |
| dc.date.available | 2020-12-26T09:26:15Z | - |
| dc.date.issued | 2020 | - |
| dc.identifier.citation | Organic Letters, 22(10), pp.3815-3819. | en_US |
| dc.identifier.other | https://doi.org/10.1021/acs.orglett.0c01056 | - |
| dc.identifier.uri | https://pubs.acs.org/doi/10.1021/acs.orglett.0c01056 | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/3387 | - |
| dc.description.abstract | A variety of cyclopropyl aryl ketones undergo uncatalyzed cascade ring-opening/recyclization reactions to generate indenones and fluorenones. In addition, a new strategy to access 3-hydroxyindanones possessing two contiguous stereogenic centers, one of them being an all-carbon quaternary center, was also established. During the course of the investigation, pronounced solvent, temperature, and substituent effects on the product distribution were discovered. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | American Chemical Society | en_US |
| dc.subject | Hydrocarbons | en_US |
| dc.subject | Pharmaceuticals | en_US |
| dc.subject | Ketones | en_US |
| dc.subject | Chemical reactions | en_US |
| dc.subject | Cyclization | en_US |
| dc.title | Ring-Opening/Recyclization Cascades of Monoactivated Cyclopropanes | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | Research Articles | |
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|---|---|---|---|---|
| need to add pdf....odt | 8.12 kB | OpenDocument Text | View/Open |
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