The Baylis-Hillman acetates as a source of ambiphilic molecules: A simple synthesis of 1,3-thiazinane-2-thione frameworks
The Baylis-Hillman acetates as a source of ambiphilic molecules: A simple synthesis of 1,3-thiazinane-2-thione frameworks
| dc.contributor.author | Basavaiah, Deevi | |
| dc.contributor.author | Pal, Sutanuka | |
| dc.contributor.author | Veeraraghavaiah, Gorre | |
| dc.contributor.author | Bharadwaj, Kishor Chandra | |
| dc.date.accessioned | 2022-03-27T09:00:53Z | |
| dc.date.available | 2022-03-27T09:00:53Z | |
| dc.date.issued | 2015-06-04 | |
| dc.description.abstract | Ambiphilic molecules (allylamines 1), easily accessible from the Baylis-Hillman acetates, have been effectively utilized for stereoselective synthesis of cis-5,6-disubstituted-1,3-thiazinane-2-thione derivatives (2) via the reaction with carbon disulfide as a bridging partner. | |
| dc.identifier.citation | Tetrahedron. v.71(28) | |
| dc.identifier.issn | 00404020 | |
| dc.identifier.uri | 10.1016/j.tet.2015.04.087 | |
| dc.identifier.uri | https://www.sciencedirect.com/science/article/abs/pii/S0040402015005979 | |
| dc.identifier.uri | https://dspace.uohyd.ac.in/handle/1/12267 | |
| dc.subject | 1,3-Thiazinane-2-thiones | |
| dc.subject | Ambiphilic molecules | |
| dc.subject | Baylis-Hillman acetates | |
| dc.subject | Bridging partner | |
| dc.subject | Carbon disulfide | |
| dc.title | The Baylis-Hillman acetates as a source of ambiphilic molecules: A simple synthesis of 1,3-thiazinane-2-thione frameworks | |
| dc.type | Journal. Article | |
| dspace.entity.type |
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