134553-38-1Relevant academic research and scientific papers
N-benzoylindole-2,3-quinodimethane: Diels-Alder reactivity and synthetic applications for [b]annellated indoles
Haber,Pindur
, p. 1925 - 1936 (2007/10/02)
The Diels-Alder reactivity of in situ generated N-benzoylindole-2,3-quinodimethane has been expanded considerably to include reactions with carbon- and hetero-dienophiles which furnish a variety of [b]annellated indoles as well as functionalized and annel
A SIMPLE ROUTE TO INDOLE-2,3-QUINODIMETHANE-A FACILE SYNTHESIS OF CARBAZOLES
Saroja, B.,Srinivasan, P. C.
, p. 5429 - 5430 (2007/10/02)
2,3-Dimethylindole is easily converted into N-benzoyl-2,3-dibromo methylindole, the latter upon treatment with sodium iodide in DMF in the presence of a suitable dienophile furnishes a carbazole derivative.
