A. A. Bredikhin, Z. A. Bredikhina, A. V. Pashagin, “Liesegang ring formation during the supramolecular hydrogelation of the chiral drug methocarbamol”, Mendeleev Commun., 2011, Volume 21, Issue 3,Pages <nobr>144

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Liesegang ring formation during the supramolecular hydrogelation of the chiral drug methocarbamol

A. A. Bredikhin, Z. A. Bredikhina, A. V. Pashagin

A.E. Arbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center of the Russian Academy of Sciences, Kazan, Russian Federation

Abstract: The chiral drug methocarbamol, which is prone to spontaneous resolution, is an effective molecular hydrogelator as both an enantiomer and a racemate; the samples of methocarbamol having an intermediate enantiomeric composition generate clearly visible periodic structures (Liesegang rings) during the gelation process.

Language: English

DOI: 10.1016/j.mencom.2011.04.010