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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