| dc.contributor.author | Clarke, Adam J. | |
| dc.contributor.author | Hunt, David A. | |
| dc.date.accessioned | 2015-06-24T15:45:19Z | |
| dc.date.available | 2015-06-24T15:45:19Z | |
| dc.date.issued | 2009-06 | |
| dc.identifier.citation | Clarke A.J.; Hunt, D.A. “β-Nitrostyrenes as Electrophiles in Parham Cyclization Chemistry. Reaction with o-Lithiobenzonitrile,” Tetrahedron Lett. 2009, 50, 2949-2951. | en_US |
| dc.identifier.uri | http://dx.doi.org/10.1016/j.tetlet.2009.03.217 | |
| dc.description | File not available for download due to copyright restrictions | en_US |
| dc.description.abstract | β-Nitrostyrenes react with o-lithiobenzonitrile, generated from the requisite aryl bromide at −100 °C by bromine–lithium exchange with n-butyllithium in THF, to afford 2-nitro-3-phenyl-3H-inden-1-ylamines resulting from 1,4-addition to the β-nitrostyrene followed by intramolecular capture of the resultant nitronate anion by the ortho-cyano functional group. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | Elsevier | en_US |
| dc.subject | Indan derivatives | en_US |
| dc.subject | Ring closure reactions | en_US |
| dc.subject | Styrene | en_US |
| dc.subject | Nitriles | en_US |
| dc.subject | Bromides | en_US |
| dc.subject | Addition reactions | en_US |
| dc.subject | Functional groups | en_US |
| dc.subject | Electrophiles | en_US |
| dc.title | β-Nitrostyrenes as Electrophiles in Parham Cyclization Chemistry. Reaction with o-Lithiobenzonitrile | en_US |
| dc.type | Article | en_US |
| dc.type | Text | en_US |
| prism.publicationName | Tetrahedron Letters | en_US |
| prism.volume | 50 | |
| prism.startingPage | 2949 | |
| prism.endingPage | 2951 | |
| dc.identifier.handle | https://dr.tcnj.edu/handle/2900/106 | |
