Show simple item record

dc.contributor.authorHunt, David A.
dc.contributor.authorCherney, Emily
dc.date.accessioned2018-09-26T20:41:52Z
dc.date.available2018-09-26T20:41:52Z
dc.date.issued2016
dc.identifier.citationCherney, E.; Hunt, D.A. “The reaction of isatoic anhydride with dimethylsulfoxide. Isolation of products formed through a putative Pummerer rearrangement” Heterocyclic Lett. 2016, 6, 591-593.en_US
dc.descriptionFile not available for download due to copyright restrictionsen_US
dc.description.abstractReaction of isatoic anhydride with dimethyl sulfoxide at 150oC results in the formation of S-methyl-2-aminobenzothioate as the result of a Pummerer rearrangement. While the reaction can be conducted in the absence of a base, yields of isolated product are higher in the presence of a base. The reaction appears to be optimal using dimethyl sulfoxide as the substrate.en_US
dc.language.isoen_USen_US
dc.publisherManind Publishing Companyen_US
dc.subjectIsatoic anhydridesen_US
dc.subjectPummerer rearrangementen_US
dc.subjectS -methyl 2- aminobenzothioatesen_US
dc.titleThe reaction of isatoic anhydride with dimethylsulfoxide. Isolation of products formed through a putative Pummerer rearrangementen_US
dc.typeArticleen_US
dc.typeTexten_US
prism.publicationNameHeterocyclic Letters
prism.publicationDate2016
prism.startingPage591
prism.endingPage593
dc.identifier.handlehttps://dr.tcnj.edu/handle/2900/2658


Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record