Chemistry of Heterocyclic Compounds.
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau.
Vol. 22.
1986.
P. 1107-1110
Arylation, alkylation, reduction, and pyrolysis of 1h-1-methylindeno[2,1-b]pyridine
Nucleophilic substitution (phenylation with phenyl lithium) of 1H-1-methylindeno[2,1-fa]pyridine 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. © 1987 Plenum Publishing Corporation.
Authors
Publisher
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Number of issue
9
Language
English
Pages
980-982
Status
Published
Link
Volume
22
Year
1986
Organizations
- 1 P. Lumumba People's Friendship University, Moscow, 117923, Russian Federation
Date of creation
19.10.2018
Date of change
19.10.2018
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Chemistry of Heterocyclic Compounds.
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau.
Vol. 22.
1986.
P. 970-976