Nucleic Acid Analogs with Constraint Conformational Flexibility in the Sugar-Phosphate Backbone ?Tricyclo-DNA?. Part 1. Preparation of [(5?R,6?R)-2?-deoxy-3?,5?-ethano-5?,6?-methano-?-D-ribofuranosyl]thymine and -adenine, and the corresponding phosphoramidites for oligonucleotide synthesis-Reference-Cited by-同舟云学术

Nucleic Acid Analogs with Constraint Conformational Flexibility in the Sugar-Phosphate Backbone ?Tricyclo-DNA?. Part 1. Preparation of [(5?R,6?R)-2?-deoxy-3?,5?-ethano-5?,6?-methano-?-D-ribofuranosyl]thymine and -adenine, and the corresponding phosphoramidites for oligonucleotide synthesis

Published:1997-12-15 Issue:8 Volume:80 Page:2426-2439
ISSN:0018-019X
Container-title:Helvetica Chimica Acta
language:de
Short-container-title:Helv. Chim. Acta

Author:

Steffans Ralph,Leumann Christian

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Biochemistry,Catalysis

Reference24 articles.

1. Chemisch modifizierte Oligonucleotide als Sonden und Agentien

2. Chemically Modified Oligonucleotides as Probes and Inhibitors

3. Antisense oligonucleotides: a new therapeutic principle

4. Current concepts in antisense drug design

5. Antisense Oligonucleotides

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