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

J 2011

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

TRÁVNÍČEK, Zdeněk, Radka NOVOTNÁ, Jaromír MAREK a Igor POPA

Základní údaje

Originální název

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

Autoři

TRÁVNÍČEK, Zdeněk, Radka NOVOTNÁ, Jaromír MAREK a Igor POPA

Vydání

Organic and Biomolecular Chemistry, Cambridge, UK, Royal Society of Chemistry, 2011, 1477-0520

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Obor

10401 Organic chemistry

Stát vydavatele

Česká republika

Utajení

není předmětem státního či obchodního tajemství

Odkazy

DOI

Impakt faktor

Impact factor: 3.696

Organizační jednotka

Přírodovědecká fakulta

UT WoS

000293230300015

Klíčová slova anglicky

CYCLIN-DEPENDENT KINASES; ADENINE NUCLEOSIDES; POTASSIUM-AMIDE; LIQUID-AMMONIA; DERIVATIVES; INHIBITORS; ADENOSINE; PURINES; COMPLEXES; MECHANISM

Příznaky

Mezinárodní význam, Recenzováno

Změněno: 2. 5. 2012 13:18, doc. RNDr. Jaromír Marek, Ph.D.

Anotace

V originále

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.

Citovat

TRÁVNÍČEK, Zdeněk, Radka NOVOTNÁ, Jaromír MAREK a Igor POPA. Transformations of the natural cytokinin N6-isopentenyladenine in aqueous acidic media: structural aspects. Organic and Biomolecular Chemistry. Cambridge, UK: Royal Society of Chemistry, 2011, roč. 9, č. 16, s. 5703-5713. ISSN 1477-0520.

@article{953907,
   author = {Trávníček, Zdeněk and Novotná, Radka and Marek, Jaromír and Popa, Igor},
   article_location = {Cambridge, UK},
   article_number = {16},
   keywords = {CYCLIN-DEPENDENT KINASES; ADENINE NUCLEOSIDES; POTASSIUM-AMIDE; LIQUID-AMMONIA; DERIVATIVES; INHIBITORS; ADENOSINE; PURINES; COMPLEXES; MECHANISM},
   language = {eng},
   issn = {1477-0520},
   journal = {Organic and Biomolecular Chemistry},
   title = {Transformations of the natural cytokinin N6-isopentenyladenine in aqueous acidic media: structural aspects},
   url = {http://pubs.rsc.org/en/Content/ArticleLanding/2011/OB/c1ob05649b},
   volume = {9},
   year = {2011}
}

TY  - JOUR
ID  - 953907
AU  - Trávníček, Zdeněk - Novotná, Radka - Marek, Jaromír - Popa, Igor
PY  - 2011
TI  - Transformations of the natural cytokinin N6-isopentenyladenine in aqueous acidic media: structural aspects
JF  - Organic and Biomolecular Chemistry
VL  - 9
IS  - 16
SP  - 5703-5713
EP  - 5703-5713
PB  - Royal Society of Chemistry
SN  - 14770520
KW  - CYCLIN-DEPENDENT KINASES
KW  - ADENINE NUCLEOSIDES
KW  - POTASSIUM-AMIDE
KW  - LIQUID-AMMONIA
KW  - DERIVATIVES
KW  - INHIBITORS
KW  - ADENOSINE
KW  - PURINES
KW  - COMPLEXES
KW  - MECHANISM
UR  - http://pubs.rsc.org/en/Content/ArticleLanding/2011/OB/c1ob05649b
N2  - 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.
ER  -

TRÁVNÍČEK, Zdeněk, Radka NOVOTNÁ, Jaromír MAREK a Igor POPA. Transformations of the natural cytokinin N6-isopentenyladenine in aqueous acidic media: structural aspects. \textit{Organic and Biomolecular Chemistry}. Cambridge, UK: Royal Society of Chemistry, 2011, roč.~9, č.~16, s.~5703-5713. ISSN~1477-0520.

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