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Macroring Opening in Crown Ethers. Transformation of (4′-Formylbenzo)thiacrown Ethers into Podands by the Action of Methylamine

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Abstract

A procedure has been developed for the synthesis of thiaaza podands from (4′-formylbenzo)thiacrown ethers via nucleophilic regioselective opening of the macroring by the action of methylamine and methylamine hydrochloride on heating.

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Translated from Zhurnal Organicheskoi Khimii, Vol. 41, No. 3, 2005, pp. 468–471.

Original Russian Text Copyright © 2005 by Dmitrieva, Churakova, Gromov.

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Dmitrieva, S.N., Churakova, M.V. & Gromov, S.P. Macroring Opening in Crown Ethers. Transformation of (4′-Formylbenzo)thiacrown Ethers into Podands by the Action of Methylamine. Russ J Org Chem 41, 461–464 (2005). https://doi.org/10.1007/s11178-005-0188-9

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  • DOI: https://doi.org/10.1007/s11178-005-0188-9

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