108576-09-6Relevant articles and documents
ARYLATION, ALKYLATION, REDUCTION, AND PYROLYSIS OF 1H-1-METHYLINDENOPYRIDINE
Soldatenkov, A. T.,Bagdadi, M. V.,Fedorov, V. O.,Prostakov, N. S.
, p. 980 - 982 (2007/10/02)
Nucleophilic substitution (phenylation with phenyl lithium) of 1H-1-methylindenopyridine occurred at the C(2) and C(4) positions, and electrophilic substitution (methylation and benzylation with halogen derivatives) at C(9).Reduction of the starting anhydrobases gave 1-methyl-1,2,3,9a-tetrahydro-1-azafluorene, and pyrolysis gave 1-azafluorene and 1-azafluorenone.