Synthesis of 2'-deoxyuridine nucleosides with appended 5-position carbonyl cross-linking groups

Article abstract of DOI:10.1080/15257779408011867

A simple modification of Stille type carbonylative coupling conditions resulted in high yield reactions giving new carbonyl appended 2'-deoxyuridine derivatives useful for chemical cross-linking.

Full text of DOI:10.1080/15257779408011867

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Nucleosides and Nucleotides
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Synthesis of 2′-Deoxyuridine Nucleosides
with Appended 5-Position Carbonyl
Cross-Linking Groups
Gregory J. Crouch a & Bruce E. Eaton a
a Department of Chemistry , Washington State University , Pullman,
Washington, 99164-4630
Published online: 24 Sep 2006.
To cite this article: Gregory J. Crouch & Bruce E. Eaton (1994) Synthesis of 2′-Deoxyuridine
Nucleosides with Appended 5-Position Carbonyl Cross-Linking Groups, Nucleosides and Nucleotides,
13:4, 939-944, DOI: 10.1080/15257779408011867
To link to this article: http://dx.doi.org/10.1080/15257779408011867
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