Publication details

Transformations of the natural cytokinin N6-isopentenyladenine in aqueous acidic media: structural aspects

Authors

TRÁVNÍČEK Zdeněk NOVOTNÁ Radka MAREK Jaromír POPA Igor

Year of publication 2011
Type Article in Periodical
Magazine / Source Organic and Biomolecular Chemistry
MU Faculty or unit

Faculty of Science

Citation
Web DOI
Field Organic chemistry
Keywords CYCLIN-DEPENDENT KINASES; ADENINE NUCLEOSIDES; POTASSIUM-AMIDE; LIQUID-AMMONIA; DERIVATIVES; INHIBITORS; ADENOSINE; PURINES; COMPLEXES; MECHANISM
Description N6-Isopentenyladenine (L1) was subjected to variously acidic media in 0.1 M, 1 M and 2 M HCl. In dependence on the acidity of the medium, the formation of three main acid hydrolysis products were determined and characterized by multinuclear solution-state NMR spectroscopy and in the solid state by single crystal X-ray analysis. The coordination abilities of these transformation products have been also investigated.

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