Literature DB >> 3186438

5'-Levulinyl and 2'-tetrahydrofuranyl protection for the synthesis of oligoribonucleotides by the phosphoramidite approach.

S Iwai1, E Ohtsuka.   

Abstract

The levulinyl group has been employed for protection of the 5'-hydroxyl group in the synthesis of oligoribonucleotides by the phosphoramidite approach, using the acid-labile 2'-tetrahydro-furanyl group. The hydrazine treatment was performed for 10 minutes in order to remove the levulinyl group on controlled pore glass. Four decaribonucleotides (AAAAAAAAAU, GGGGGGGGGU, CCCCCCCCCU and UUUUUUUUUU) and a heneicosamer (GCCUAGCUGAUGAAGGGUGAU) were prepared with an automatic synthesizer in good yields.

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Year:  1988        PMID: 3186438      PMCID: PMC338755          DOI: 10.1093/nar/16.20.9443

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  12 in total

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3.  Studies on the sequence of the 3'-terminal region of turnip-yellow-mosaic-virus RNA.

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5.  DNA sequence analysis: a general, simple and rapid method for sequencing large oligodeoxyribonucleotide fragments by mapping.

Authors:  E Jay; R Bambara; R Padmanabhan; R Wu
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7.  Solid-phase synthesis of oligoribonucleotides.

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Authors:  N D Sinha; J Biernat; J McManus; H Köster
Journal:  Nucleic Acids Res       Date:  1984-06-11       Impact factor: 16.971

9.  A new solid-phase synthesis of oligoribonucleotides by the phosphoro-p-anisidate method using tetrahydrofuranyl protection of 2'-hydroxyl groups.

Authors:  S Iwai; E Yamada; M Asaka; Y Hayase; H Inoue; E Ohtsuka
Journal:  Nucleic Acids Res       Date:  1987-05-11       Impact factor: 16.971

10.  Solid-phase synthesis of polynucleotides. III. Synthesis of polynucleotides with defined sequences by the block coupling phosphotriester method.

Authors:  K Miyoshi; T Huang; K Itakura
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  12 in total

1.  Chemical synthesis of biologically active oligoribonucleotides using beta-cyanoethyl protected ribonucleoside phosphoramidites.

Authors:  S A Scaringe; C Francklyn; N Usman
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2.  Chemical synthesis of the 24 RNA fragments corresponding to hop stunt viroid.

Authors:  H Tanimura; M Maeda; T Fukazawa; M Sekine; T Hata
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3.  Use of synthetic oligoribonucleotides to probe RNA-protein interactions in the MS2 translational operator complex.

Authors:  S J Talbot; S Goodman; S R Bates; C W Fishwick; P G Stockley
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4.  Forks and combs and DNA: the synthesis of branched oligodeoxyribonucleotides.

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5.  Solid-phase synthesis of oligoribonucleotides using 9-fluorenylmethoxycarbonyl (Fmoc) for 5'-hydroxyl protection.

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7.  A convenient approach to the synthesis of medium size oligodeoxyribonucleotides by improved new phosphite method.

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8.  Synthesis and applications of oligoribonucleotides with selected 2'-O-methylation using the 2'-O-[1-(2-fluorophenyl)-4-methoxypiperidin-4-yl] protecting group.

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9.  Use of new phosphonylating and coupling agents in the synthesis of oligodeoxyribonucleotides via the H-phosphonate approach.

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10.  Binding of nucleic acids to E. coli RNase HI observed by NMR and CD spectroscopy.

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