Rapid, catalyst free, solid phase modification of DNA by strain promoted cyclooctyne-nitrile oxide click chemistry is reported; the reaction is characterised by mild conditions, occurring in an aqueous environment under atmospheric conditions at room temperature and is complete in 10 minutes
Solid-phase oligonucleotide conjugation by nitrile oxide-alkyne click cycloaddition chemistry has be...
Solid-phase oligonucleotide conjugation by nitrile oxide–alkyne click cycloaddition chemistry has b...
Solid-phase oligonucleotide conjugation by nitrile oxide–alkyne click cycloaddition chemistry has b...
Rapid, catalyst free, solid phase modification of DNA by strain promoted cyclooctyne-nitrile oxide c...
Rapid, catalyst free, solid phase modification of DNA by strain promoted cyclooctyne-nitrile oxide c...
Biocompatible, strain promoted cyclooctyne–nitrile oxide click chemistry is demonstrated as a rapid ...
Biocompatible, strain promoted cyclooctyne–nitrile oxide click chemistry is demonstrated as a rapid ...
Biocompatible, strain promoted cyclooctyne–nitrile oxide click chemistry is demonstrated as a rapid ...
Biocompatible, strain promoted cyclooctyne–nitrile oxide click chemistry is demonstrated as a rapid ...
Strain promoted cycloaddition is presented as a tool for RNA conjugation on the solid phase; RNA-cyc...
Strain promoted cycloaddition is presented as a tool for RNA conjugation on the solid phase; RNA-cyc...
Strain promoted cycloaddition is presented as a tool for RNA conjugation on the solid phase; RNA-cyc...
Strain promoted cycloaddition is presented as a tool for RNA conjugation on the solid phase; RNA-cy...
Strain promoted cycloaddition is presented as a tool for RNA conjugation on the solid phase; RNA-cy...
Strain promoted cycloaddition is presented as a tool for RNA conjugation on the solid phase; RNA-cy...
Solid-phase oligonucleotide conjugation by nitrile oxide-alkyne click cycloaddition chemistry has be...
Solid-phase oligonucleotide conjugation by nitrile oxide–alkyne click cycloaddition chemistry has b...
Solid-phase oligonucleotide conjugation by nitrile oxide–alkyne click cycloaddition chemistry has b...
Rapid, catalyst free, solid phase modification of DNA by strain promoted cyclooctyne-nitrile oxide c...
Rapid, catalyst free, solid phase modification of DNA by strain promoted cyclooctyne-nitrile oxide c...
Biocompatible, strain promoted cyclooctyne–nitrile oxide click chemistry is demonstrated as a rapid ...
Biocompatible, strain promoted cyclooctyne–nitrile oxide click chemistry is demonstrated as a rapid ...
Biocompatible, strain promoted cyclooctyne–nitrile oxide click chemistry is demonstrated as a rapid ...
Biocompatible, strain promoted cyclooctyne–nitrile oxide click chemistry is demonstrated as a rapid ...
Strain promoted cycloaddition is presented as a tool for RNA conjugation on the solid phase; RNA-cyc...
Strain promoted cycloaddition is presented as a tool for RNA conjugation on the solid phase; RNA-cyc...
Strain promoted cycloaddition is presented as a tool for RNA conjugation on the solid phase; RNA-cyc...
Strain promoted cycloaddition is presented as a tool for RNA conjugation on the solid phase; RNA-cy...
Strain promoted cycloaddition is presented as a tool for RNA conjugation on the solid phase; RNA-cy...
Strain promoted cycloaddition is presented as a tool for RNA conjugation on the solid phase; RNA-cy...
Solid-phase oligonucleotide conjugation by nitrile oxide-alkyne click cycloaddition chemistry has be...
Solid-phase oligonucleotide conjugation by nitrile oxide–alkyne click cycloaddition chemistry has b...
Solid-phase oligonucleotide conjugation by nitrile oxide–alkyne click cycloaddition chemistry has b...
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