Issue 34, 2014

New water soluble Pd-imidate complexes as highly efficient catalysts for the synthesis of C5-arylated pyrimidine nucleosides

Abstract

The direct reactions between the precursors trans-[Pd(imidate)2(SMe2)2] and 1,3,5-triaza-7-phosphaadamantane (PTA) yield new water-soluble palladium(II) complexes trans-[Pd(imidate)2(PTA)2](imidate = succinimidate (suc) 1, maleimidate (mal) 2, phthalimidate (phthal) 3 or saccharinate (sacc) 4. The new complexes were revealed as excellent catalysts for environmentally friendly, efficient Suzuki–Miyaura cross-coupling of synthetically challenging substrates like the antiviral nucleoside analogue 5-iodo-2′-deoxyuridine in water as solvent.

Graphical abstract: New water soluble Pd-imidate complexes as highly efficient catalysts for the synthesis of C5-arylated pyrimidine nucleosides

Supplementary files

Article information

Article type
Paper
Submitted
14 Feb 2014
Accepted
31 Mar 2014
First published
31 Mar 2014

RSC Adv., 2014,4, 17567-17572

Author version available

New water soluble Pd-imidate complexes as highly efficient catalysts for the synthesis of C5-arylated pyrimidine nucleosides

A. Kapdi, V. Gayakhe, Y. S. Sanghvi, J. García, P. Lozano, I. da Silva, J. Pérez and J. L. Serrano, RSC Adv., 2014, 4, 17567 DOI: 10.1039/C4RA01326C

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