Issue 7, 2013

Improved microwave-assisted ligand-free Suzuki–Miyaura cross-coupling of 5-iodo-2′-deoxyuridine in pure water

Abstract

A facile and efficient methodology for direct synthesis of 5-aryl-2′-deoxyuridines was developed through ligand-free Suzuki–Miyaura cross-coupling reactions starting from totally deprotected 5-iodo-2′-deoxyuridine and various boronic acids. Reactions were performed, in pure water, in the presence of very low loading of palladium either by classical thermal heating or with the assistance of microwave irradiation yielding 5-arylated uridine derivatives in moderate to good yields within short reaction times.

Graphical abstract: Improved microwave-assisted ligand-free Suzuki–Miyaura cross-coupling of 5-iodo-2′-deoxyuridine in pure water

Supplementary files

Article information

Article type
Paper
Submitted
13 Feb 2013
Accepted
04 Apr 2013
First published
04 Apr 2013

New J. Chem., 2013,37, 1989-1995

Improved microwave-assisted ligand-free Suzuki–Miyaura cross-coupling of 5-iodo-2′-deoxyuridine in pure water

S. Gallagher-Duval, G. Hervé, G. Sartori, G. Enderlin and C. Len, New J. Chem., 2013, 37, 1989 DOI: 10.1039/C3NJ00174A

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