Towards novel amide-modified oligonucleotides: asymmetric synthesis of 5′-(S)-methyl-3′-carboxymethylene-3′-deoxythymidine-Reference-Cited by-同舟云学术

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Towards novel amide-modified oligonucleotides: asymmetric synthesis of 5′-(S)-methyl-3′-carboxymethylene-3′-deoxythymidine

Published:2002-07 Issue:31 Volume:43 Page:5461-5464
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Wendeborn Sebastian,Nussbaumer Hannes,Robert Frédéric,Jörg Mario,Pachlatko Johannes Paul

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference23 articles.

1. Synthesis of thymidine dimer derivatives containing an amide linkage and their incorporation into oligodeoxyribonucleotides

2. Amides as a New Type of Backbone Modification in Oligonucleotides

3. Synthesis and hybridization properties of amide-linked thymidine dimers incorporated into oligodeoxynucleotides

4. Antisense Oligonucleotides

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2. The Krapcho Dealkoxycarbonylation Reaction of Esters with α-Electron-Withdrawing Substituents;Organic Reactions;2013-05-30

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5. Studies on 2′-α-C-carboxyalkyl nucleosides and their application to a stereocontrolled nucleobase exchange process;Org. Biomol. Chem.;2003

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