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Synthesis of New Tripodal Hydroxybenzoic Esters and their Reaction with Tris-(2-aminoethyl)amine under High Pressure Conditions

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The new simple method of synthesis of tripodal esters, building blocks for monomacrocyclic pendant macrocycles and bicyclic cryptands is reported. Six new tripodal esters, derivatives of hydroxybenzoic acids were prepared and characterized, and their reaction with tris(2-aminoethyl)amine carried under high pressure conditions was studied using Electrospray Ion Mass Spectrometry





Keywords: Electrospray Ion Mass Spectrometry; High pressure synthesis; amine; bicyclic cryptands; cryptands; hydroxybenzoic acids; lariat compounds; pendant macrocycles; pressure; tripodal esters

Document Type: Research Article

Publication date: 01 February 2012

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  • Letters in Organic Chemistry publishes original letters on all areas of organic chemistry including synthesis, bioorganic, medicinal, natural products, organometallic, supramolecular, molecular recognition and physical organic chemistry. The emphasis is placed on publishing quality papers very rapidly. Letters are processed rapidly and take full advantage of the Internet technology both for the submission and the review of the manuscripts.
    The journal is essential reading for all organic chemists both in academia and industry.
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