Synthesis of thiazolidine-thiones, imino-thiazolidines and oxazolidines: Via the base promoted cyclisation of epoxy-sulfonamides and heterocumulenes

dc.contributor.author Anitha, Mandala
dc.contributor.author Swamy, K. C.Kumara
dc.date.accessioned 2022-03-27T09:48:09Z
dc.date.available 2022-03-27T09:48:09Z
dc.date.issued 2018-01-01
dc.description.abstract Epoxy-sulfonamides react with heterocumulenes (carbon disulfide/isothiocyanates/isocyanates) in the presence of a base to afford ring expansion products in good to high yields with excellent regioselectivity. N-(2-Bromoethyl)-sulfonamides can also be employed as substrates. This reaction proceeds through a 5-exo-tet pathway without forming aziridine intermediates.
dc.identifier.citation Organic and Biomolecular Chemistry. v.16(3)
dc.identifier.issn 14770520
dc.identifier.uri 10.1039/c7ob02915b
dc.identifier.uri http://xlink.rsc.org/?DOI=C7OB02915B
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/13320
dc.title Synthesis of thiazolidine-thiones, imino-thiazolidines and oxazolidines: Via the base promoted cyclisation of epoxy-sulfonamides and heterocumulenes
dc.type Journal. Article
dspace.entity.type
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