Dimethyl sulfide induced [3 + 2] annulation strategy: An efficient synthesis of functionalized dihydropyrazole derivatives using the Baylis-Hillman bromides
Dimethyl sulfide induced [3 + 2] annulation strategy: An efficient synthesis of functionalized dihydropyrazole derivatives using the Baylis-Hillman bromides
| dc.contributor.author | Basavaiah, Deevi | |
| dc.contributor.author | Roy, Suparna | |
| dc.date.accessioned | 2022-03-27T09:01:50Z | |
| dc.date.available | 2022-03-27T09:01:50Z | |
| dc.date.issued | 2008-05-01 | |
| dc.description.abstract | Baylis-Hlllman bromides have been successfully employed as a valuable source of 1,3-dipoles for cycloaddition onto dialkyl azodicarboxylates (dipolarophiles) under the influence of dimethyl sulfide and potassium carbonate to provide functionalized dihydropyrazole derivatives in a simple one-pot [3 + 2] annulation strategy. © 2008 American Chemical Society. | |
| dc.identifier.citation | Organic Letters. v.10(9) | |
| dc.identifier.issn | 15237060 | |
| dc.identifier.uri | 10.1021/ol800424v | |
| dc.identifier.uri | https://pubs.acs.org/doi/10.1021/ol800424v | |
| dc.identifier.uri | https://dspace.uohyd.ac.in/handle/1/12296 | |
| dc.title | Dimethyl sulfide induced [3 + 2] annulation strategy: An efficient synthesis of functionalized dihydropyrazole derivatives using the Baylis-Hillman bromides | |
| dc.type | Journal. Article | |
| dspace.entity.type |
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