The Baylis-Hillman acetates as a valuable source for one-pot multistep synthesis: A facile synthesis of functionalized tri-/tetracyclic frameworks containing azocine moiety
The Baylis-Hillman acetates as a valuable source for one-pot multistep synthesis: A facile synthesis of functionalized tri-/tetracyclic frameworks containing azocine moiety
| dc.contributor.author | Basavaiah, Deevi | |
| dc.contributor.author | Aravindu, Kunche | |
| dc.date.accessioned | 2022-03-27T09:01:55Z | |
| dc.date.available | 2022-03-27T09:01:55Z | |
| dc.date.issued | 2007-06-21 | |
| dc.description.abstract | The Baylis-Hillman acetates have been conveniently transformed into tri-/tetracyclic heterocyclic frameworks containing an important azocine moiety via one-pot multistep protocol involving alkylation, reduction, and cyclization sequence. © 2007 American Chemical Society. | |
| dc.identifier.citation | Organic Letters. v.9(13) | |
| dc.identifier.issn | 15237060 | |
| dc.identifier.uri | 10.1021/ol070380u | |
| dc.identifier.uri | https://pubs.acs.org/doi/10.1021/ol070380u | |
| dc.identifier.uri | https://dspace.uohyd.ac.in/handle/1/12298 | |
| dc.title | The Baylis-Hillman acetates as a valuable source for one-pot multistep synthesis: A facile synthesis of functionalized tri-/tetracyclic frameworks containing azocine moiety | |
| dc.type | Journal. Article | |
| dspace.entity.type |
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