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Synthesis of Nucleobase-Modified RNA Oligonucleotides by Post-Synthetic Approach

Molecules (Basel, Switzerland), 2020-07, Vol.25 (15), p.3344

2020

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2-Selenouridine, a Modified Nucleoside of Bacterial tRNAs, Its Reactivity in the Presence of Oxidizing and Reducing Reagents

International journal of molecular sciences, 2022-07, Vol.23 (14), p.7973

2022

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C5-Substituted 2-Selenouridines Ensure Efficient Base Pairing with Guanosine; Consequences for Reading the NNG-3' Synonymous mRNA Codons

International journal of molecular sciences, 2020-04, Vol.21 (8), p.2882

2020

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Different Oxidation Pathways of 2-Selenouracil and 2-Thiouracil, Natural Components of Transfer RNA

International journal of molecular sciences, 2020-08, Vol.21 (17), p.5956

2020

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The influence of the C5 substituent on the 2-thiouridine desulfuration pathway and the conformational analysis of the resulting 4-pyrimidinone products

Bioorganic & medicinal chemistry, 2015-09, Vol.23 (17), p.5587-5594

2015

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Efficient access to 3′-O-phosphoramidite derivatives of tRNA related N6-threonylcarbamoyladenosine (t6A) and 2-methylthio-N6-threonylcarbamoyladenosine (ms2t6A)

RSC advances, 2021-01, Vol.11 (4), p.1992-1999

2021

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Efficient conversion of N 6 -threonylcarbamoyladenosine (t 6 A) into a tRNA native hydantoin cyclic form (ct 6 A) performed at nucleoside and oligoribonucleotide levels

Chemical communications (Cambridge, England), 2017-07, Vol.53 (56), p.7945-7948

2017

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Post-synthetic conversion of 5-pivaloyloxymethyluridine present in a support-bound RNA oligomer into biologically relevant derivatives of 5-methyluridine

Organic & biomolecular chemistry, 2017-03, Vol.15 (9), p.2097-2103

2017

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Chemical Synthesis of Oligoribonucleotide (ASL of tRNALys T. brucei) Containing a Recently Discovered Cyclic Form of 2‐Methylthio‐N6‐threonylcarbamoyladenosine (ms2ct6A)

Chemistry : a European journal, 2019-10, Vol.25 (58), p.13309-13317

2019

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Chemical Synthesis of Oligoribonucleotide (ASL of tRNALys T. brucei) Containing a Recently Discovered Cyclic Form of 2‐Methylthio‐N6‐threonylcarbamoyladenosine (ms2ct6A)

Chemistry : a European journal, 2019-10, Vol.25 (58), p.13228-13228

2019

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Novel entry to the synthesis of ()- and ()-5-methoxycarbonylhydroxymethyluridines - a diastereomeric pair of wobble tRNA nucleosides

RSC advances, 2019-12, Vol.9 (69), p.457-4512

2019

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S-Geranylated 2-Thiouridines of Bacterial tRNAs: Chemical Synthesis and Physicochemical Properties

European journal of organic chemistry, 2016-07, Vol.2016 (21), p.3482-3485

2016

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DNA binding and cleavage studies of copper(II) complexes with 2′-deoxyadenosine modified histidine moiety

Journal of biological inorganic chemistry, 2015-09, Vol.20 (6), p.989-1004

2015

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Desulfuration of 2-thiouridine with hydrogen peroxide in the physiological pH range 6.6–7.6 is pH-dependent and results in two distinct products

Bioorganic & medicinal chemistry letters, 2013-11, Vol.23 (21), p.5803-5805

2013

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Transformation of a wobble 2-thiouridine to 2-selenouridine via S-geranyl-2-thiouridine as a possible cellular pathway

Bioorganic chemistry, 2014-10, Vol.56, p.49-53

2014

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Reaction of S-geranyl-2-thiouracil modified oligonucleotides with alkyl amines leads to the N2-alkyl isocytosine derivatives

Organic & biomolecular chemistry, 2017-06, Vol.15 (25), p.5332-5336

2017

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Uracil ring opening in the reaction of 5-formyl-2′-deoxyuridine with primary alkyl amines

Tetrahedron letters, 2007-02, Vol.48 (8), p.1363-1367

2007

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Efficient synthesis of 2′-deoxyzebularine and its α-anomer by the silyl method of N-glycosylation. Crystal structures and conformational study in solution

Carbohydrate research, 2014-06, Vol.392, p.7-15

2014

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The 2-thiouridine unit in the RNA strand is desulfured predominantly to 4-pyrimidinone nucleoside under in vitro oxidative stress conditions

Chemical communications (Cambridge, England), 2011-05, Vol.47 (17), p.4914-4916

2011

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An efficient approach for conversion of 5-substituted 2-thiouridines built in RNA oligomers into corresponding desulfured 4-pyrimidinone products

Bioorganic & medicinal chemistry letters, 2015-08, Vol.25 (16), p.3100-3104

2015

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RNA-cleaving 10–23 deoxyribozyme with a single amino acid-like functionality operates without metal ion cofactors

New journal of chemistry, 2010, Vol.34 (5), p.934-948

2010

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Efficient desulfurization of 2-thiopyrimidine nucleosides to the corresponding 4-pyrimidinone analogues using trans-2-(phenylsulfonyl)-3-phenyloxaziridine

Tetrahedron letters, 2004-08, Vol.45 (36), p.6729-6731

2004

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Impact of histidine residue on chelating ability of 2′-deoxyriboadenosine

Journal of inorganic biochemistry, 2011-09, Vol.105 (9), p.1212-1219

2011

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Histamine modified 2′-deoxyriboadenosine – Potential copper binding site in DNAzymes

Journal of inorganic biochemistry, 2010-05, Vol.104 (5), p.570-575

2010

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Desulfurization of 2-thiouracil nucleosides: Conformational studies of 4-pyrimidinone nucleosides

Bioorganic & medicinal chemistry, 2011-04, Vol.19 (7), p.2443-2449

2011

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Synthesis of Nucleobase-Modified RNA Oligonucleotides by Post-Synthetic Approach

2-Selenouridine, a Modified Nucleoside of Bacterial tRNAs, Its Reactivity in the Presence of Oxidizing and Reducing Reagents

C5-Substituted 2-Selenouridines Ensure Efficient Base Pairing with Guanosine; Consequences for Reading the NNG-3' Synonymous mRNA Codons

Different Oxidation Pathways of 2-Selenouracil and 2-Thiouracil, Natural Components of Transfer RNA

The influence of the C5 substituent on the 2-thiouridine desulfuration pathway and the conformational analysis of the resulting 4-pyrimidinone products

Efficient access to 3′-O-phosphoramidite derivatives of tRNA related N6-threonylcarbamoyladenosine (t6A) and 2-methylthio-N6-threonylcarbamoyladenosine (ms2t6A)

Efficient conversion of N 6 -threonylcarbamoyladenosine (t 6 A) into a tRNA native hydantoin cyclic form (ct 6 A) performed at nucleoside and oligoribonucleotide levels

Post-synthetic conversion of 5-pivaloyloxymethyluridine present in a support-bound RNA oligomer into biologically relevant derivatives of 5-methyluridine

Chemical Synthesis of Oligoribonucleotide (ASL of tRNALys T. brucei) Containing a Recently Discovered Cyclic Form of 2‐Methylthio‐N6‐threonylcarbamoyladenosine (ms2ct6A)

Chemical Synthesis of Oligoribonucleotide (ASL of tRNALys T. brucei) Containing a Recently Discovered Cyclic Form of 2‐Methylthio‐N6‐threonylcarbamoyladenosine (ms2ct6A)

Novel entry to the synthesis of ()- and ()-5-methoxycarbonylhydroxymethyluridines - a diastereomeric pair of wobble tRNA nucleosides

S-Geranylated 2-Thiouridines of Bacterial tRNAs: Chemical Synthesis and Physicochemical Properties

DNA binding and cleavage studies of copper(II) complexes with 2′-deoxyadenosine modified histidine moiety

Desulfuration of 2-thiouridine with hydrogen peroxide in the physiological pH range 6.6–7.6 is pH-dependent and results in two distinct products

Transformation of a wobble 2-thiouridine to 2-selenouridine via S-geranyl-2-thiouridine as a possible cellular pathway

Reaction of S-geranyl-2-thiouracil modified oligonucleotides with alkyl amines leads to the N2-alkyl isocytosine derivatives

Uracil ring opening in the reaction of 5-formyl-2′-deoxyuridine with primary alkyl amines

Efficient synthesis of 2′-deoxyzebularine and its α-anomer by the silyl method of N-glycosylation. Crystal structures and conformational study in solution

The 2-thiouridine unit in the RNA strand is desulfured predominantly to 4-pyrimidinone nucleoside under in vitro oxidative stress conditions

An efficient approach for conversion of 5-substituted 2-thiouridines built in RNA oligomers into corresponding desulfured 4-pyrimidinone products

RNA-cleaving 10–23 deoxyribozyme with a single amino acid-like functionality operates without metal ion cofactors

Efficient desulfurization of 2-thiopyrimidine nucleosides to the corresponding 4-pyrimidinone analogues using trans-2-(phenylsulfonyl)-3-phenyloxaziridine

Impact of histidine residue on chelating ability of 2′-deoxyriboadenosine

Histamine modified 2′-deoxyriboadenosine – Potential copper binding site in DNAzymes

Desulfurization of 2-thiouracil nucleosides: Conformational studies of 4-pyrimidinone nucleosides

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