α-phenylisocinchomeronic and 4-azafluorenone 3-carboxylic acids

3,6-Dimethyl-6-phenylpyridine, obtained on phenylation of 2,5-lutidine, has been used in the synthesis of α-phenylisocinchomeronic acid, derivatives of it, and also for the preparation of 4-azafluorenone 3-carboxylic acid. It was established that 4-hydroxy-3,6-dimethyl-2-phenylpyridine was formed on phenylation of 2,5-lutidine. © 1986 Plenum Publishing Corporation.

Publisher
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Number of issue
5
Language
English
Pages
529-532
Status
Published
Volume
22
Year
1986
Organizations
  • 1 P. Lumumba Peoples' Friendship University, Moscow, Russian Federation
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Other records

Shevtsov V.K., Varlamov A.V., Poshivalov S.G., Simonova L.A., Prostakov N.S.
Chemistry of Heterocyclic Compounds. Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau. Vol. 22. 1986. P. 577-580
Proatakov N.S., Kirillova L.M., Habib H.B., Murugova L.A.
Chemistry of Heterocyclic Compounds. Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau. Vol. 22. 1986. P. 200-205