(Q61836111)

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A convenient synthesis of S-cyanoethyl-protected 4-thiouridine and its incorporation into oligoribonucleotides

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A convenient synthesis of S-cyanoethyl-protected 4-thiouridine and its incorporation into oligoribonucleotides (English)

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author name string

Chris J. Adams

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1

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James B. Murray

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2

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John R.P. Arnold

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3

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Peter G. Stockley

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4

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publication date

January 1994

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published in

Tetrahedron Letters

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volume

35

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issue

5

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page(s)

765-768

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cites work

The Functionalization of Oligonucleotides Via Phosphoramidite Derivatives

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Antisense oligonucleotides: a new therapeutic principle

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4'-Thio-oligo-beta-D-ribonucleotides: synthesis of beta-4'-thio-oligouridylates, nuclease resistance, base pairing properties, and interaction with HIV-1 reverse transcriptase

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Synthesis of a 4-thio-2'-deoxyuridine containing oligonucleotide. Development of the thiocarbonyl group as a linker element.

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A small catalytic oligoribonucleotide

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Chemical synthesis of a biologically active natural tRNA with its minor bases

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Prevention of chain cleavage in the chemical synthesis of 2'-silylated oligoribonucleotides

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Chemical synthesis of RNA using fast oligonucleotide deprotection chemistry

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High-performance liquid chromatographic analysis of oligodeoxyribonucleotide base composition

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The role of the exocyclic amino groups of conserved purines in hammerhead ribozyme cleavage

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10.1016/S0040-4039(00)75812-6

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(Q61836111)

A convenient synthesis of S-cyanoethyl-protected 4-thiouridine and its incorporation into oligoribonucleotides

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