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The synthesis of oligonucleotides that contain 2,4-dinitrophenyl reporter groups

✍ Scribed by David W. Will; Clare E. Pritchard; Tom Brown


Publisher
Elsevier Science
Year
1992
Tongue
English
Weight
585 KB
Volume
216
Category
Article
ISSN
0008-6215

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✦ Synopsis


The synthesis of non-nucleoside-based phosphoramidites that bear the 2,4-dinitrophenyl group is reported. These labelled phosphoramidites, which have been used in solid-phase oligonucleotide synthesis to attach single and multiple dinitrophenyl groups to the 5'-end of oligonucleotides, are entirely compatible with the normal oligonucleotide synthesis cycle. Multiple labelling can be performed readily in high yield and the resulting oligonucleotides can be purified readily by reversed-phase h.p.l.c. The labelled oligonucleotides have been detected using monoclonal and polyclonal anti-dinitrophenyl antibodies.


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## Abstract Cyclohexyl nucleosides with an adenine and uracil base have been synthesized from 2‐azidocyclohexane‐1,5‐diol. The obtained racemic nucleosides were resolved using (__R__)‐__O__‐methylmandelic acid. Short oligonucleotides were synthesized using phorphoramidite chemistry. However, these