Nucleotides. Part XLI . The 2‐dansylethoxycarbonyl (  2‐{[5‐(dimethylamino)naphthalen‐1‐yl]sulfonyl}ethoxycarbonyl; dnseoc) group for protection of the 5′‐hydroxy function in oligodeoxyribonucleotide synthesis | Zendy

Bergmann Frank | Zendy; Pfleiderer Wolfgang | Zendy

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Nucleotides. Part XLI . The 2‐dansylethoxycarbonyl (  2‐{[5‐(dimethylamino)naphthalen‐1‐yl]sulfonyl}ethoxycarbonyl; dnseoc) group for protection of the 5′‐hydroxy function in oligodeoxyribonucleotide synthesis

Author(s) -

Bergmann Frank,

Pfleiderer Wolfgang

Publication year - 1994

Publication title -

helvetica chimica acta

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.74

H-Index - 82

eISSN - 1522-2675

pISSN - 0018-019X

DOI - 10.1002/hlca.19940770123

Subject(s) - chemistry , sulfonyl , phosphoramidite , protecting group , stereochemistry , nucleotide , group (periodic table) , combinatorial chemistry , organic chemistry , oligonucleotide , biochemistry , dna , alkyl , gene

Use of the 2‐dansylethoxycarbonyl ( 2‐{[5‐(dimethylamino)naphthalen‐1‐yl]sulfonyl}ethoxycarbonyl; Dnseoc) group as an intermediate 5′‐OH protecting group in oligodeoxyribonucleotide synthesis using the automated phosphoramidite approach is described in a model study to an alternative strategy in RNA synthesis.

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