Deconvoluting the reactivity of two intermediates formed from modified pyrimidines. - Wikidata - awgldk - TriplyDB

Deconvoluting the reactivity of two intermediates formed from modified pyrimidines.

Deconvoluting the reactivity of two intermediates formed from modified pyrimidines.

http://www.wikidata.org/entity/Q37316554

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Reactivity of Nucleic Acid Radicals.Interstrand cross-link and bioconjugate formation in RNA from a modified nucleotide.Bromopyridone Nucleotide Analogues, Anoxic Selective Radiosensitizing Agents That Are Incorporated in DNA by Polymerases.DNA interstrand cross-linking upon irradiation of aryl halide C-nucleotides.Photochemical Generation of Benzyl Cations That Selectively Cross-Link Guanine and Cytosine in DNA.Pyrimidine Nucleobase Radical Reactivity in DNA and RNA.Independent Generation and Reactivity of Thymidine Radical Cations.

P2860

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Deconvoluting the reactivity of two intermediates formed from modified pyrimidines.

http://www.wikidata.org/entity/Q37316554

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 03 July 2013

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Deconvoluting the reactivity of two intermediates formed from modified pyrimidines.

@en

Deconvoluting the reactivity of two intermediates formed from modified pyrimidines.

@nl

type

label

Deconvoluting the reactivity of two intermediates formed from modified pyrimidines.

@en

Deconvoluting the reactivity of two intermediates formed from modified pyrimidines.

@nl

prefLabel

Deconvoluting the reactivity of two intermediates formed from modified pyrimidines.

@en

Deconvoluting the reactivity of two intermediates formed from modified pyrimidines.

@nl

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Organic Letters

P1476

Deconvoluting the reactivity of two intermediates formed from modified pyrimidines.

@en

P2093

Carl H Schiesser

http://www.w3.org/2001/XMLSchema#string

Liwei Weng

http://www.w3.org/2001/XMLSchema#string

Marc M Greenberg

http://www.w3.org/2001/XMLSchema#string

Sonia M Horvat

http://www.w3.org/2001/XMLSchema#string

P2860

DNA interstrand cross-link formation initiated by reaction between singlet oxygen and a modified nucleotide

Nucleophilic reactivities of hydrazines and amines: the futile search for the α-effect in hydrazine reactivities.

Oxygen independent DNA interstrand cross-link formation by a nucleotide radical.

Photochemical generation and reactivity of the major hydroxyl radical adduct of thymidine

Hypoxia-selective DNA interstrand cross-link formation by two modified nucleosides

Radicals masquerading as electrophiles: dual orbital effects in nitrogen-philic acyl radical cyclization and related addition reactions.

The chemistry of single-stranded 4'-DNA radicals: influence of the radical precursor on anaerobic and aerobic strand cleavage.

Oxidation and reduction of the 5-(2'-deoxyuridinyl)methyl radical

Multinuclear NMR and kinetic analysis of DNA interstrand cross-link formation.

Efficient DNA interstrand cross-link formation from a nucleotide radical.

P304

3618-3621

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scholarly article

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10.1021/OL401472M

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14

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15

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2013-07-03T00:00:00Z

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23822109

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3830933

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