Solid-phase oligonucleotide conjugation by nitrile oxide–alkyne click cycloaddition chemistry has been successfully demonstrated; the reaction, compatible with all nucleobases, requires no metal catalyst and proceeds under physiological conditions
The advent of click chemistry has led to an influx of new ideas in the nucleic acids field. The copp...
The need for precise and flexible synthetic methodology to underpin modern research in chemical biol...
'Click' chemistry has been widely applied in nucleic acid studies, the most common reactions being t...
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...
Solid-phase oligonucleotide conjugation by nitrile oxide–alkyne click cycloaddition chemistry has b...
A fast and practical metal free conjugation of ribonucleosides and 2¢-OMe 4-mer oligoribonucleotides...
Solid-phase oligonucleotide conjugation by nitrile oxide-alkyne click cycloaddition chemistry has be...
Conjugation of ligands to DNA oligonucleotides has been achieved in the solid phase by strain-promot...
Biocompatible, strain promoted cyclooctyne–nitrile oxide click chemistry is demonstrated as a rapid ...
The need for precise and flexible synthetic methodology to underpin modern research in chemical biol...
Chemoselective ligation of biologically significant moieties through azide alkyne Click Chemistry h...
A fast and practical metal free conjugation of ribonucleosides and 2¢-OMe 4-mer oligoribonucleotides...
The versatility of the isoxazole generating nitrile oxide–alkyne Huisgen cycloaddition for provision...
A fast and practical metal free conjugation of ribonucleosides and 2'-OMe 4-mer oligoribonucleotides...
The advent of click chemistry has led to an influx of new ideas in the nucleic acids field. The copp...
The need for precise and flexible synthetic methodology to underpin modern research in chemical biol...
'Click' chemistry has been widely applied in nucleic acid studies, the most common reactions being t...
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...
Solid-phase oligonucleotide conjugation by nitrile oxide–alkyne click cycloaddition chemistry has b...
A fast and practical metal free conjugation of ribonucleosides and 2¢-OMe 4-mer oligoribonucleotides...
Solid-phase oligonucleotide conjugation by nitrile oxide-alkyne click cycloaddition chemistry has be...
Conjugation of ligands to DNA oligonucleotides has been achieved in the solid phase by strain-promot...
Biocompatible, strain promoted cyclooctyne–nitrile oxide click chemistry is demonstrated as a rapid ...
The need for precise and flexible synthetic methodology to underpin modern research in chemical biol...
Chemoselective ligation of biologically significant moieties through azide alkyne Click Chemistry h...
A fast and practical metal free conjugation of ribonucleosides and 2¢-OMe 4-mer oligoribonucleotides...
The versatility of the isoxazole generating nitrile oxide–alkyne Huisgen cycloaddition for provision...
A fast and practical metal free conjugation of ribonucleosides and 2'-OMe 4-mer oligoribonucleotides...
The advent of click chemistry has led to an influx of new ideas in the nucleic acids field. The copp...
The need for precise and flexible synthetic methodology to underpin modern research in chemical biol...
'Click' chemistry has been widely applied in nucleic acid studies, the most common reactions being t...
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