The Baylis-Hillman reaction: TiCl < inf > 4 < /inf > mediated coupling of alkyl vinyl ketones with α-keto esters and aldehydes
The Baylis-Hillman reaction: TiCl < inf > 4 < /inf > mediated coupling of alkyl vinyl ketones with α-keto esters and aldehydes
| dc.contributor.author | Basavaiah, D. | |
| dc.contributor.author | Sreenivasulu, B. | |
| dc.contributor.author | Reddy, R. M. | |
| dc.contributor.author | Muthukumaran, K. | |
| dc.date.accessioned | 2022-03-27T09:03:26Z | |
| dc.date.available | 2022-03-27T09:03:26Z | |
| dc.date.issued | 2001-01-01 | |
| dc.description.abstract | TiCl4 mediated coupling of alkyl vinyl ketones with α-keto esters and aldehydes provides respectively 2-aryl-2-hydroxy-3-methylene-4-oxoalkanoates and (Z)-keto allyl chlorides in 1 h time at room temperature. Similar coupling of trifluoromethyl phenyl ketone with methyl vinyl ketone produces 1,1,1-trifluoro-2-hydroxy-2-phenyl-3-methylenepentan-4-one. | |
| dc.identifier.citation | Synthetic Communications. v.31(19) | |
| dc.identifier.issn | 00397911 | |
| dc.identifier.uri | 10.1081/SCC-100105670 | |
| dc.identifier.uri | http://www.tandfonline.com/doi/abs/10.1081/SCC-100105670 | |
| dc.identifier.uri | https://dspace.uohyd.ac.in/handle/1/12343 | |
| dc.title | The Baylis-Hillman reaction: TiCl < inf > 4 < /inf > mediated coupling of alkyl vinyl ketones with α-keto esters and aldehydes | |
| dc.type | Journal. Article | |
| dspace.entity.type |
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