162825-34-5Relevant articles and documents
Ab initio calculations of effect of (thio)xanthenyl and dibenzosuberenyl substituents on dehydrogenation of N-Benzylanilines
Yunnikova,Feshin,Akent'Eva
, p. 703 - 707 (2013/07/27)
Higher values of the energies of the highest occupied molecular orbitals for N-benzyl-4-[9-(thio)-xanthenyl]aniline, N-benzyl-4-(5-dibenzosuberenyl) aniline molecules and their zwitterions and the electron density increase on the reaction center (carbon a
Reactions of N-Benzylideneanilines with Xanthene
Yunnikova, L. P.
, p. 67 - 70 (2007/10/03)
Reactions of N-benzylideneanilines with xanthene in trifluoroacetic acid yield N-benzyl-4-(xanthen-9-yl)anilines and/or N-benzylidene-4-(xanthen-9-yl)anilines, N-benzylanilines, and a dimeric product, 1,9'-bixanthene, depending on the nature and position of the substituent, the solvent nature, the reactant ratio, and the temperature.