Synthesis of [15 N4 ] purine labeled cytokinin glycosides derived from zeatins and topolins with 9-β-d, 7-β-d-glucopyranosyl, or 9-β-d-ribofuranosyl group
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
IGA_LF_2018_032
Palacký University - International
IGA_PrF_2018_029
Palacký University - International
CZ.01.1.02/0.0/0.0/15_019/0004431
OP PIK - International
TE02000058
TAČR - International
PubMed
30592529
DOI
10.1002/jlcr.3702
Knihovny.cz E-zdroje
- Klíčová slova
- cytokinins, internal standard, labeled adenine, labeled purine, topolin, zeatin,
- MeSH
- adenin analogy a deriváty MeSH
- izotopy dusíku chemie MeSH
- zeatin analogy a deriváty MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- adenin MeSH
- izotopy dusíku MeSH
- zeatin MeSH
Synthesis of [15 N4 ] purine labeled cytokinine glycosides derived from zeatins and topolins containing a 9-β-d, 7-β-d-glucopyranosyl, or 9-β-d-ribofuranosyl group is described. These N6 -substituted adenine derivatives are intended as internal analytic standards for phytohormone analysis. All labeled compounds were prepared from 6-chloro[15 N4 ]purine (1). The equilibrium reaction of 1 with acetobromo-α-d-glucose gave isomeric 7-β-d (3) and 9-β-d (4) chloro glucosyl precursors, which were treated with the corresponding amines to get desired labeled cytokinin 7-β-d (6) and 9-β-d (5) glucopyranosides. Cytokinins containing 9-β-d-ribofuranosyl group (8) were obtained by direct enzymatic transglycosylation reaction of cytokinins (7) prepared from 6-chloro[15 N4 ] purine (1).
Citace poskytuje Crossref.org
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