| dc.contributor.author | Hunt, David A. | |
| dc.contributor.author | Bertonazzi, Joanne | |
| dc.contributor.author | Thornton, Sarah | |
| dc.contributor.author | Grossman, Alec | |
| dc.date.accessioned | 2018-10-17T20:46:08Z | |
| dc.date.available | 2018-10-17T20:46:08Z | |
| dc.date.issued | 2016 | |
| dc.identifier.citation | Bertonazzi, J.; Thornton, S.; Grossman, A.; Hunt, D.A. “Reaction of functionalized aryllithium reagents with N-alkylisatoic anhydrides. A straightforward route to 2’ substituted 2-N-alkylaminobenzophenone derivatives,” Heterocyclic Lett. 2016, 6, 423 427. | en_US |
| dc.description | File not available for download due to copyright restrictions | en_US |
| dc.description.abstract | N-Substituted isatoic anhydrides have been found to cleanly undergo acylation with Parham reagents (highly elctrophillic
functional group-substituted aryllithium reagents) followed by elimination of CO2 to afford novel 2’-substituted 2-N-alkyl-aminobenzophenones difficult to prepare by standard methods. Such derivatives could prove useful as intermediates toward the
preparation of novel heterocyclic systems. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | Manind Publishing Company | en_US |
| dc.title | Reaction of Functionalized Aryllithium Reagents with N-Alkylisatoic Anhydrides. A Straight forward Route to 2’-Substituted 2-N-Alkylaminobenzophenone Derivatives | en_US |
| dc.type | Article | en_US |
| dc.type | Text | en_US |
| prism.publicationName | Heterocyclic Letters | |
| prism.volume | 6 | |
| prism.publicationDate | 2016 | |
| prism.startingPage | 423 | |
| dc.identifier.handle | https://dr.tcnj.edu/handle/2900/2685 | |
