Synthesis of an enantiomerically pure carbocyclic DNA abasic site analogue

DOI: 10.1080/15257779908043071

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Nucleosides and Nucleotides p. 239 - 243 (1999)

Update date:2022-09-26

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Authors:

Thomas, Martial

Castaing, Bertrand

Fourrey, Jean-Louis

Zelwer, Charles

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Article abstract of DOI:10.1080/15257779908043071

A short synthetic route to an appropriately derivatized carbocyclic analogue of a basic site residues of DNA is proposed.

Full text of DOI:10.1080/15257779908043071

Nucleosides and Nucleotides

ISSN: 0732-8311 (Print) (Online) Journal homepage: http://www.tandfonline.com/loi/lncn19

Synthesis of an Enantiomerically Pure Carbocyclic

DNA Abasic Site Analogue

Martial Thomas , Bertrand Castaing , Jean-Louis Fourrey & Charles Zelwer

To cite this article: Martial Thomas , Bertrand Castaing , Jean-Louis Fourrey & Charles

Zelwer (1999) Synthesis of an Enantiomerically Pure Carbocyclic DNA Abasic Site Analogue,

Nucleosides and Nucleotides, 18:2, 239-243, DOI: 10.1080/15257779908043071

To link to this article: http://dx.doi.org/10.1080/15257779908043071

Published online: 04 Oct 2006.

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Article Doi

Synthesis of an enantiomerically pure carbocyclic DNA abasic site analogue

DOI: 10.1080/15257779908043071

Source and publish data:

Authors:

Article abstract of DOI:10.1080/15257779908043071

Full text of DOI:10.1080/15257779908043071

Products guided by the article

R&D Labs maybe for 221258-61-3

Relevant to this article

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Simple oxidation of 3-O-silylated glycals: Application in deblocking 3-0-protected glycals

DESULFONYLATION OF β-KETO SULFONES WITH THE HANTZSCH ESTER, AN NAD(P)H MODEL

The use of liquid phase carriers for large scale oligonucleotide synthesis in solution via phosphoamidite chemistry

Preparation of Substituted Phenanthridines from the Coupling of Aryldiazonium Salts with Nitriles: A Metal Free Approach