scispace - formally typeset
Journal ArticleDOI

2′(3′),5′-Diphosphate des Nucleosids X und N3-alkylierter Uridin–Derivate

Frank Seela, +1 more
- 01 Nov 1979 - 
- Vol. 112, Iss: 11, pp 3743-3747
Reads0
Chats0
TLDR
In this paper, the synthesis of 2′(3′),5′-diphosphates of the rare nucleoside X (1a) and the N3 - alkylated uridine derivatives 1b, c, and 2b has been accomplished by treatement of the nucleosides with 15 fold excess pyrophosphoryl chloride.
Abstract
2′(3′), 5′-Diphosphates of the Nucleoside X and N3 - Alkylated Uridine Derivatives The synthesis of 2′(3′),5′-diphosphates of the rare nucleoside X (1a) and the N3 - alkylated uridine derivatives 1b, c, and 2b has been accomplished by treatement of the nucleosides with 15 fold excess pyrophosphoryl chloride.

read more

Citations
More filters
Book ChapterDOI

5-AZA-7-Deazapurines: Synthesis and Properties of Nucleosides and Oligonucleotides

TL;DR: In this article, the synthesis and properties of base-modified purine nucleosides with a nitrogen atom in a bridgehead position were discussed, and the synthesis of 5-aza-7-deazapurines can be performed either by a linear or a convergent route.
References
More filters
Journal ArticleDOI

Synthesis of modified nucleoside 3′,5′-bisphosphates and their incorporation into oligoribonucleotides with T4 RNA ligase

TL;DR: A simple procedure is described to prepare nucleoside 3'(2'),5'-bisphosphates from the corresponding nucleosides with the use of pyrophosphoryl chloride, which is rapid, gives nearly quantitative yields and, most importantly, can be used for a variety of nucleosided with base and sugar modifications.
Journal ArticleDOI

Equimolar addition of oligoribonucleotides with T4 RNA ligase.

TL;DR: The data suggest that T4 RNA ligase will be a useful enzyme for the synthesis of oligomers of defined sequence.
Journal ArticleDOI

Joining of 3'-modified oligonucleotides by T4 RNA ligase. Synthesis of a heptadecanucleotide corresponding to the bases 61--77 from Escherichia coli tRNAfMet.

TL;DR: The 3' terminus of C-C-A was modified by introduction of the ethoxymethylidene group to prevent intra- and intermolecular self-joining reactions at the 3' end to yield a heptadecanucleotide.
Journal ArticleDOI

Darstellung und Eigenschaften von N3‐(3‐L‐Amino‐3‐carboxypropyl)uridin‐5′‐monophosphat – einem modifizierten Nucleotid aus Transfer‐RNA

TL;DR: In this paper, a modified nucleotide from transfer RNA was obtained by alkylation of isopropylideneuridine with ethyl α-L-benzamidoγ-bromobutyrate and after removal of the protecting groups from the intermediate 4.