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rdf:type
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Description
| - The H-1 and C-13 NMR resonances of 16 purine glucosides were assigned by a combination of one- and two-dimensional NMR experiments, including gs-COSY, gs-HSQC, and gs-HMBC, in order to characterize the effect of substituent and the position of glucose unit on the NMR chemical shifts. In addition, N-15 NMR chemical shifts for selected derivatives were investigated by using H-1-N-15 chemical shift correlation techniques. To map the influence of sugar moiety on the directly bonded nitrogen atom, selected N-9-glucosides and their ribose analogs were compared. Characteristic long-range H-1-N-15 coupling constants, measured by using H-1-N-15 gradient-selected single-quantum multiple bond correlation (GSQMBC), are also reported and discussed. All compounds investigated here belong to cytokinins, an important group of plant hormones.
- The H-1 and C-13 NMR resonances of 16 purine glucosides were assigned by a combination of one- and two-dimensional NMR experiments, including gs-COSY, gs-HSQC, and gs-HMBC, in order to characterize the effect of substituent and the position of glucose unit on the NMR chemical shifts. In addition, N-15 NMR chemical shifts for selected derivatives were investigated by using H-1-N-15 chemical shift correlation techniques. To map the influence of sugar moiety on the directly bonded nitrogen atom, selected N-9-glucosides and their ribose analogs were compared. Characteristic long-range H-1-N-15 coupling constants, measured by using H-1-N-15 gradient-selected single-quantum multiple bond correlation (GSQMBC), are also reported and discussed. All compounds investigated here belong to cytokinins, an important group of plant hormones. (en)
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Title
| - H-1-, C-13-, and N-15-NMR chemical shifts for selected glucosides and ribosides of aromatic cytokinins
- H-1-, C-13-, and N-15-NMR chemical shifts for selected glucosides and ribosides of aromatic cytokinins (en)
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skos:prefLabel
| - H-1-, C-13-, and N-15-NMR chemical shifts for selected glucosides and ribosides of aromatic cytokinins
- H-1-, C-13-, and N-15-NMR chemical shifts for selected glucosides and ribosides of aromatic cytokinins (en)
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skos:notation
| - RIV/61389030:_____/10:00359282!RIV11-GA0-61389030
|
http://linked.open...avai/riv/aktivita
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http://linked.open...avai/riv/aktivity
| - P(GA301/08/1649), S, Z(AV0Z50380511), Z(MSM0021622413), Z(MSM6198959216)
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http://linked.open...iv/cisloPeriodika
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http://linked.open...vai/riv/dodaniDat
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http://linked.open...aciTvurceVysledku
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http://linked.open.../riv/druhVysledku
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http://linked.open...iv/duvernostUdaju
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http://linked.open...titaPredkladatele
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http://linked.open...dnocenehoVysledku
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http://linked.open...ai/riv/idVysledku
| - RIV/61389030:_____/10:00359282
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http://linked.open...riv/jazykVysledku
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http://linked.open.../riv/klicovaSlova
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http://linked.open.../riv/klicoveSlovo
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http://linked.open...odStatuVydavatele
| - GB - Spojené království Velké Británie a Severního Irska
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http://linked.open...ontrolniKodProRIV
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http://linked.open...i/riv/nazevZdroje
| - Magnetic Resonance in Chemistry
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http://linked.open...in/vavai/riv/obor
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http://linked.open...ichTvurcuVysledku
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http://linked.open...cetTvurcuVysledku
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http://linked.open...vavai/riv/projekt
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http://linked.open...UplatneniVysledku
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http://linked.open...v/svazekPeriodika
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http://linked.open...iv/tvurceVysledku
| - Strnad, Miroslav
- Maloň, Michal
- Marek, R.
- Vícha, J.
- Humpa, O.
- Veselá, P.
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http://linked.open...ain/vavai/riv/wos
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http://linked.open...n/vavai/riv/zamer
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issn
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number of pages
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is http://linked.open...avai/riv/vysledek
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