Abstract
9-Substituted 2,6-dichlorojulolidines and 1-aryl-2,5-di(chloromethyl)pyrrolidines-alkylating compounds with alkylating centers in fixed positions — were synthesized, and their basicities and rates of hydrolysis were determined. The relationship between the structure, basicity, and rate of hydrolysis of these compounds is discussed.
This is a preview of subscription content, log in via an institution to check access.
Similar content being viewed by others
Literature cited
J. J. Roberts and W. C. J. Ross, J. Chem. Soc., 4289 (1952).
S. N. Borodulina and S. V. Sokolov, Zh. Organ, Khim., 2, 1088 (1966).
S. N. Borodulina and S. V. Sokolov, Khim. Geterotsikl. Soedin., 626 (1970).
N. N. Vorozhtsov and S. I. Kutkevichus, Zh. Obshch. Khim., 27, 2152 (1957).
S. W. Blackmann and R. Baltzly, J. Org. Chem., 25, 2750 (1961).
V. R. Boehme and E. S. Schipper, US Patent No. 3,006,920 (1959); Referativnyi Zh. Khim., 4N89 (1963).
D. P. Dubinskaite and Yu. A. Degutis, Material from the 18th Scientific-Technical Conference [in Russian], Kaunas (1968), p. 69.
Yu. A. Degutis and D. P. Dubinskaite, Zh. Obshch. Khim., 1003 (1970).
W. C. J. Ross, J. Chem. Soc., 183 (1949).
J. F. Coetzee and S. R. Padnanbhan, J. Am. Chem. Soc., 87, 5005 (1965).
V. I. Bren', “Basicities and structures of azomethines and their structural analogs,” Author's Abstract of Dissertation [in Russian], Rostov-on-Don (1969).
J. L. Everett and W. C. J. Ross, J. Chem. Soc., 1972 (1949).
Author information
Authors and Affiliations
Additional information
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 41–44, January, 1972.
Rights and permissions
About this article
Cite this article
Degutis, Y., Dubinskaite, D. Investigation of 2,6-dichlorojulolidines and 1-aryl-2,5-di(chloromethyl)pyrrolidines. Chem Heterocycl Compd 8, 39–42 (1972). https://doi.org/10.1007/BF00478488
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF00478488