Abstract
The effect has been studied of the nature of the substituent (methyl, chloro, nitro group) on the Fischer cyclization of 5-substituted pyrid-2-yl-hydrazones of cyclohexanone under the action of different catalysts: Lewis acids and strong mineral and arylsulfonic acids.
Similar content being viewed by others
References
L. N. Yakhontov, E. V. Pronina, and M. V. Rubtsov, DAN, 169, 361, 1966.
L. N. Yakhontov, E. V. Pronina, and M. V. Rubtsov, KhGS [Chemistry of Heterocyclic Compounds], 687, 1967.
H. L. Bradlow and C. A. Vanderwerf, J. Org. Chem., 1, 509, 1949.
A. E. Chichibabin and A. F. Egorov, ZhRKhO, 60, 683, 1928.
A. Mangini and B. Freguelli, Gazz. chim. ital., 69, 97, 1939.
K. T. Potts and H. R. Burton, J. Org. Chem., 31, 251, 1966.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Yakhontov, L.N., Pronina, E.V. & Rubtsov, M.V. Fischer cyclization of 5-substituted pyrid-2-yl-hydrazones of cyclohexanone. Chem Heterocycl Compd 6, 170–174 (1970). https://doi.org/10.1007/BF00474990
Issue Date:
DOI: https://doi.org/10.1007/BF00474990