Alkylation-Elimination Reaction in Quaternary Ammonium Salts

Torosyan Gh
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Torosyan Gh: National polytechnic university of Armenia, Yerevan

Organic & Medicinal Chemistry International Journal, 2017, vol. 3, issue 3, 76-77

Abstract: During our work on the alkylation of organic acids containing carbonyl groups - as β-diketones [1,2], it was decided to study the possibility of alkylation of quaternary ammonium salts (QUAT) such as trimethylphenacyl ammonium bromide [3]. We have proceeded from the fact that such QUAT can’t undergoes to Hofmann elimi-nation or on rearrangements (Sommele-Hauser, Stevens) also under this type of milder basic conditions.

Keywords: juniper publishers:Medicinal Chemistry; Biochemistry Journal; Pharmacology Journal; biochemical pharmacology; molecular pharmacology; biochemistry; open access journals; peer reviewed journals; Open Access; Journal of Molecular Biochemistry; International Research Journal of Pure and Applied Chemistry; World Journal of Biological Chemistry; Biochemistry and Analytical Biochemistry; Biochemistry & Physiology: Open Access; Molecular Biology International; Plant Biochemistry & Physiology; International Journal of Molecular Sciences; Journal of Clinical and Medical Genomics; Environmental Analytical Chemistry; Medicinal Chemistry; Juniper publishers reivews (search for similar items in EconPapers)
Date: 2017
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Persistent link: https://EconPapers.repec.org/RePEc:adp:jomcij:v:3:y:2017:i:3:p:76-77

DOI: 10.19080/OMCIJ.2017.03.555613

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