Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5274220 | Tetrahedron Letters | 2008 | 4 Pages |
Abstract
An alternative route for the synthesis of a photoaffinity labelling (PAL) dCTP derivative is reported. This method involves the intermediacy of exo-N-[2-(4-azido-2,3,5,6-tetrafluorobenzamido)ethyl]-dC. The latter is prepared from the coupling of known N-(2-aminoethyl)-4-azido-2,3,5,6-tetrafluorobenzamide, prepared in an improved three-step sequence, with an activated 4-triazolyl derivative of dU, followed by deprotection. 19F NMR spectroscopy proved extremely useful in following the synthetic transformations, and enabled control of any adventitious reduction of the azides.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Crina CismaÅ, Thanasis Gimisis,