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New, Efficient Approach for the Ligand-Free Suzuki–Miyaura Reaction of 5-Iodo-2′-deoxyuridine in Water
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2013
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Chemical EngineeringCross-coupling ReactionLigand-free ProcessEngineeringNatural SciencesDiversity-oriented SynthesisEfficient ApproachOrganic ChemistryOrganometallic CatalysisSynthetic ChemistryChemistryLigand-free Suzuki–miyaura ReactionHeterocycle ChemistryShort Reaction TimesNeat Water
A series of 5-aryl-2′-deoxyuridines was prepared, using ligandless Suzuki–Miyaura cross-coupling reactions in neat water, starting from 5-iodo-2′-deoxyuridine as totally deprotected starting material. This ligand-free process gave good to high isolated yields within short reaction times and with low loadings of palladium.