K. Turgunov, D. Kadirova, R. Okmanov
Dec 31, 2019
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Journal
European Journal of Chemistry
Abstract
Structures of alkaloid convolvine (1) isolated from Convolvulus subhirsutus and its derivatives-convolamine( N -methylconvolvine) (2) and hydrochloride of N -benzylconvolvine (3) have been determined by single crystal X-ray diffraction technique. Compounds were crystallized in monoclinic space groups having four molecules in unit cell. All compounds contain a bicyclic ring system of tropane, where piperidine rings in all case adopt chair conformation. Hydrogen atom and methyl- and benzyl-substituents located in nitrogen atom of studied compounds occupy equatorial positions. The substituent of tropane core- the veratroyloxy group containing in all compound molecules is an α-axial oriented relative to the tropane core. In crystal structures of compound 1 and 2, the molecules are located in the distance of van der Waals interactions. The H-bond between the anion Cl and the proton of the N atom is observed in the crystal of N -benzylconvolvine hydrochloride (Cl···N 3.337 A, Cl···H 2.42 A and Cl-H-N 175°).