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rdf:type
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Description
| - At pH lower than 5 under conditions of d.c. polarography and cyclic voltammetry the oxime PhCOC(=NOH)CH3 does not yield the expected reducible alpha-aminoketone, but rather a non-reducible olefin derivative. Its formation is attributed to a reduction of a diprotonated form of a ketoimine intermediate. In the same pH-range under conditions of controlled potential electrolysis the olefin derivative is slowly converted in a homogeneous reaction into a reducible alpha-aminoketone.
- At pH lower than 5 under conditions of d.c. polarography and cyclic voltammetry the oxime PhCOC(=NOH)CH3 does not yield the expected reducible alpha-aminoketone, but rather a non-reducible olefin derivative. Its formation is attributed to a reduction of a diprotonated form of a ketoimine intermediate. In the same pH-range under conditions of controlled potential electrolysis the olefin derivative is slowly converted in a homogeneous reaction into a reducible alpha-aminoketone. (en)
- Na rozdíl od izomérního oximu Ph-C(=NOH)-C(=O)-CH3 nevzniká při polarografické a voltametrické redukci oximu Ph-C(=O)-C(=NOH)-CH3 za pH < 5 očekávaný a dále redukovatelný α-aminoketon, ale neredukovatelný olefin Ph-C(OH)=C(NH2)-CH3. Jeho tvorba je přisouzena redukci diprotonované formy ketoiminového derivátu, který je stabilizován pouze jednou substituční variantou. Tento enolový produkt však není zcela stálý a pomalu konvertuje na příslušný aminoketon, jehož redukce se projeví pouze v dlouhotrvající elektrolýze. (cs)
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Title
| - Reduction of two isomeric oximes of aryl alkyl 1,2-diketones: Difference in products formed in polarography and controlled potential electrolysis
- Reduction of two isomeric oximes of aryl alkyl 1,2-diketones: Difference in products formed in polarography and controlled potential electrolysis (en)
- Redukce dvou izomerních oximů aryl alkyl 1,2-diketonů: Rozdíl v produktech vzniklých při polarografii a při potenciostatické elektrolýze (cs)
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skos:prefLabel
| - Reduction of two isomeric oximes of aryl alkyl 1,2-diketones: Difference in products formed in polarography and controlled potential electrolysis
- Reduction of two isomeric oximes of aryl alkyl 1,2-diketones: Difference in products formed in polarography and controlled potential electrolysis (en)
- Redukce dvou izomerních oximů aryl alkyl 1,2-diketonů: Rozdíl v produktech vzniklých při polarografii a při potenciostatické elektrolýze (cs)
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skos:notation
| - RIV/61388955:_____/06:00085396!RIV08-MSM-61388955
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http://linked.open.../vavai/riv/strany
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http://linked.open...avai/riv/aktivita
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http://linked.open...avai/riv/aktivity
| - P(1P05ME785), Z(AV0Z40400503)
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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/61388955:_____/06:00085396
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http://linked.open...riv/jazykVysledku
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http://linked.open.../riv/klicovaSlova
| - polarography; cyclic voltammetry; controlled potential electrolysis (en)
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http://linked.open.../riv/klicoveSlovo
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http://linked.open...odStatuVydavatele
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http://linked.open...ontrolniKodProRIV
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http://linked.open...i/riv/nazevZdroje
| - Electrochemistry Communications
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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
| - Ludvík, Jiří
- Celik, H.
- Zuman, P.
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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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