A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä
Hydrolysis and intramolecular transesterification of ribonucleoside 3 '-phosphotriesters: the effect of alkyl groups on the general and specific acid-base-catalyzed reactions of 5 '-O-pivaloyluridin-3 '-yl dialkyl phosphates
Tekijät: Kosonen M, Hakala K, Lonnberg H
Kustantaja: ROYAL SOC CHEMISTRY
Julkaisuvuosi: 1998
Lehti:: Royal Society of Chemistry. Journal: Perkin Transactions 2
Tietokannassa oleva lehden nimi: JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2
Lehden akronyymi: J CHEM SOC PERK T 2
Numero: 3
Aloitussivu: 663
Lopetussivu: 670
Sivujen määrä: 8
ISSN: 0300-9580
DOI: https://doi.org/10.1039/a707095k
Tiivistelmä
Diisopropyl, diethyl, bis(2-methoxyethyl) and isopropyl 2-methoxyethyl esters of 5'-pivaloyl-2'-(tetrahydropyran-2-yl)uridin-3'-yl phosphate have been prepared. The 2'-protecting group has been removed under acidic conditions, and the isomerization of the resulting ribonucleoside 3'-phosphotriester to its 2'-counterpart and the cleavage of the isomeric mixture to 2'- and 3'-phosphodiesters and a 2',3'-cyclic phosphate has been followed by reverse phase HPLC in aqueous hydrogen chloride and several buffer solutions over a wide acidity range from H-0 - 1.5 to pH 8. The beta(1g) values of the buffer-independent partial reactions, and the beta(1g) and Bronsted alpha and beta values of the buffer catalyzed reactions have been determined. The mechanisms of various partial reactions are discussed on the basis of the structural effects observed.
Diisopropyl, diethyl, bis(2-methoxyethyl) and isopropyl 2-methoxyethyl esters of 5'-pivaloyl-2'-(tetrahydropyran-2-yl)uridin-3'-yl phosphate have been prepared. The 2'-protecting group has been removed under acidic conditions, and the isomerization of the resulting ribonucleoside 3'-phosphotriester to its 2'-counterpart and the cleavage of the isomeric mixture to 2'- and 3'-phosphodiesters and a 2',3'-cyclic phosphate has been followed by reverse phase HPLC in aqueous hydrogen chloride and several buffer solutions over a wide acidity range from H-0 - 1.5 to pH 8. The beta(1g) values of the buffer-independent partial reactions, and the beta(1g) and Bronsted alpha and beta values of the buffer catalyzed reactions have been determined. The mechanisms of various partial reactions are discussed on the basis of the structural effects observed.
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