Abstract
The reactivity of Amberlite (IRA-67) base "heterogeneous" resin in Sonogashira cross-coupling of 8-bromoguanosine 1 with phenylacetylene 3 to give 2 has been examined. Both 1 and 2 coordinate to Pd and Cu ions, which explains why at equivalent catalyst loadings, the homogeneous reaction employing triethylamine base is poor yielding. X-ray photo-electron spectroscopy (XPS) has been used to probe and quantify the active nitrogen base sites of the Amberlite resin, and postreaction Pd and Cu species. The Pd2Cl3(PPh)2 precatalyst and CuI cocatalyst degrade to give Amberlite-supported metal nanoparticles (average size ∼2.7 nm). The guanosine product 2 formed using the Amberlite Pd/Cu catalyst system is of higher purity than reactions using a homogeneous Pd precatalyst, a prerequisite for use in biological applications.
Original language | English |
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Pages (from-to) | 168-184 |
Number of pages | 17 |
Journal | Nucleosides, Nucleotides and Nucleic Acids |
Volume | 30 |
Issue number | 2 |
Early online date | 24 Dec 2010 |
DOIs | |
Publication status | Published - 2011 |
Keywords
- nucleoside
- alkyne
- palladium
- cross-coupling
- inhibition
- catalyst recycling