dc.contributor.author | Hunt, David A. | |
dc.contributor.author | Cherney, Emily | |
dc.date.accessioned | 2018-09-26T20:41:52Z | |
dc.date.available | 2018-09-26T20:41:52Z | |
dc.date.issued | 2016 | |
dc.identifier.citation | Cherney, 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.description | File not available for download due to copyright restrictions | en_US |
dc.description.abstract | Reaction 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.iso | en_US | en_US |
dc.publisher | Manind Publishing Company | en_US |
dc.subject | Isatoic anhydrides | en_US |
dc.subject | Pummerer rearrangement | en_US |
dc.subject | S -methyl 2- aminobenzothioates | en_US |
dc.title | The reaction of isatoic anhydride with dimethylsulfoxide. Isolation of products formed through a putative Pummerer rearrangement | en_US |
dc.type | Article | en_US |
dc.type | Text | en_US |
prism.publicationName | Heterocyclic Letters | |
prism.publicationDate | 2016 | |
prism.startingPage | 591 | |
prism.endingPage | 593 | |
dc.identifier.handle | https://dr.tcnj.edu/handle/2900/2658 | |