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synthesis of γ-monolactones of 2,7-dialkyl-2,7-diamino-4-hydroxyoctane-1,8-dioic acids and their 4-methyl-substituted derivatives
Authors:M. A. Manukyan  A. A. Akhnazaryan  S. M. Asikyan  M. T. Dangyan
Affiliation:(1) Yerevan State University, 375049 Yerevan
Abstract:gamma-Monolactones of 2,7-dialkyl-2,7-diamino-4-hydroxyoctane-1,8-dioic acids and their 4-methyl-substituted derivatives were synthesized by the Gabriel reaction from the appropriate agr, agrprime-dichlorolactone esters, which are formed by cyclization (catalytically with H2SO4 or thermally) of 2,7-dialkyl-2,7-dichloro-4-octene-1,8-dioic acids or their 4-methyl-substituted derivatives and subsequent esterification of the acid grouping.Translated from Khimiya Geterotsiklichesikikh Soedinenii, No. 4, pp. 453–455, April, 1977.
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