Synthesis of fluorescent adenosine analogues

Article abstract of DOI:10.1080/15257779508012379

In the synthesis of a transition state inhibitor of the enzyme adenylosuccinate lyase two different [2,1-i]-pyrimido-purine derivatives are formed, of which one might be very interesting for cell biological research, due to its strong fluorescent properties.

Full text of DOI:10.1080/15257779508012379

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Nucleosides and Nucleotides
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Synthesis of Fluorescent Adenosine
Analogues1
R. F. de Boer a , D. G. I. Petra a , M. J. Wanner a , A. Boesaart a & G.
J. Koomen a
a Laboratory of Organic Chemistry , University of Amsterdam ,
Nieuwe Achtergracht 129, 1018, WS, Amsterdam, The Netherlands
Published online: 16 Feb 2007.
To cite this article: R. F. de Boer , D. G. I. Petra , M. J. Wanner , A. Boesaart & G. J. Koomen (1995)
Synthesis of Fluorescent Adenosine Analogues1 , Nucleosides and Nucleotides, 14:3-5, 349-352
To link to this article: http://dx.doi.org/10.1080/15257779508012379
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