In situ formed acetals facilitated direct Michael addition of unactivated ketones
In situ formed acetals facilitated direct Michael addition of unactivated ketones
| dc.contributor.author | Koppolu, Srinivasa Rao | |
| dc.contributor.author | Balamurugan, Rengarajan | |
| dc.date.accessioned | 2022-03-27T08:39:12Z | |
| dc.date.available | 2022-03-27T08:39:12Z | |
| dc.date.issued | 2017-01-01 | |
| dc.description.abstract | TfOH-promoted synthesis of 1,5-diketones by the Michael reaction of unactivated ketones with chalcones has been described. Acetals formed under HC(OMe)3/TfOH conditions generate the required enol-equivalents for a smooth Michael reaction. A wide array of symmetrical and unsymmetrical 1,5-diketones has been synthesised. | |
| dc.identifier.citation | New Journal of Chemistry. v.41(3) | |
| dc.identifier.issn | 11440546 | |
| dc.identifier.uri | 10.1039/C6NJ02954J | |
| dc.identifier.uri | http://xlink.rsc.org/?DOI=C6NJ02954J | |
| dc.identifier.uri | https://dspace.uohyd.ac.in/handle/1/11373 | |
| dc.title | In situ formed acetals facilitated direct Michael addition of unactivated ketones | |
| dc.type | Journal. Article | |
| dspace.entity.type |
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