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More recent work on the regioselective Suzuki coupling of 4,5-dibromothiophene-2-carboxaldehyde also exhibits this same dehalogenation after initial coupling at C5 when DMF is employed as the solvent. It should also be noted that no dehalogenation is observed in either the thiophene or pyridine series in DMF in the absence of a boronic acid.
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More recent work on the regioselective Suzuki coupling of 4,5-dibromothiophene-2-carboxaldehyde also exhibits this same dehalogenation after initial coupling at C5 when DMF is employed as the solvent. It should also be noted that no dehalogenation is observed in either the thiophene or pyridine series in DMF in the absence of a boronic acid.
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