81054-82-2Relevant academic research and scientific papers
The Reaction of Aryl Azides with 1,4-Quinones
Barnish, Ian T.,Gibson, Martin S.
, p. 1740 - 1757 (2007/10/02)
Aryl azides react with 1,4-quinones to give adducts which undergo one or both of the following reactions in situ: (a) dehydrogenation to the corresponding quinone or (b) denitrogenation with accompanying rearrangement to the corresponding enamine of the 2,5-dioxo-3-cyclopentene-1-carbaldehyde or 1,3-dioxoindan-2-carbaldehyde, as appropriate.
Extremely Reactive C=C Double Bonds, VI. - Tris(methylphenylamino)methane - The Chemistry of Orthoamides
Schoenberg, Alexander,Singer, Erich,Stephan, Werner
, p. 1581 - 1588 (2007/10/02)
Reactions of the title compound 2 with sulfur, selenium, thiophenol, malononitrile, 1,3-indanedione, fluorenone hydrazone, phenylmagnesium bromide, bromine, thioacetic acid, N,N'-diphenylurea, oxalyl chloride, 9,9-dichloroxanthene, phenyl isocyanate, and stilbene dibromide are described and the mechanisms are discussed.The catalytic influence of 2 on the decomposition of 9-diazofluorene in xylene and mesitylene is discussed.
