Palladium-mediated coupling reactions of an amino-substituted heterocycle. Direct synthesis of C-nucleosides related to adenosine

Article abstract of DOI:10.1080/15257779508014656

C-Nucleosides of the pyrazolo [1,5-a]-1,3,5-triazine aglycon system have been prepared by palladium-mediated coupling of 8-iodopyrazolo[1,5-a]-1,3,5-triazines. 4-(N,N'-Diisobutyloxycarbonyl)amino-8-iodopyrazolo[1,5-a]-1,3, 5-triazi ne and the furanoid gly

Full text of DOI:10.1080/15257779508014656

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Nucleosides and Nucleotides
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Palladium-Mediated Coupling
Reactions of an Aminosubstituted
Heterocycle. Direct Synthesis of C-
Nucleosides Related to Adenosine
Han-Cheng Zhang a , Mohamed Brakta a & G. Doyle Daves Jr. a
a Department of Chemistry, Rensselaer Polytechnic Institute,
Troy, New York, 12180
Version of record first published: 24 Sep 2006.
To cite this article: Han-Cheng Zhang, Mohamed Brakta & G. Doyle Daves Jr. (1995): Palladium-
Mediated Coupling Reactions of an Aminosubstituted Heterocycle. Direct Synthesis of C-
Nucleosides Related to Adenosine, Nucleosides and Nucleotides, 14:1-2, 105-116
To link to this article: http://dx.doi.org/10.1080/15257779508014656
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