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J. Org. Chem. In The Journal of Organic Chemistry, Vol. 77, No. 20. (24 September 2012), pp. 9384-9390, doi:10.1021/jo3015837 Key: citeulike:11864621
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An effective Pd(0) carbene complex was successfully employed in the decarboxylative coupling of the heteroaromatic carboxylic acids (imidazo[1,2-a]pyridine and isoxazole) with aryl halides. For carboxyindoles, either decarboxylative coupling or tandem C?H arylation and decarboxylation occurred, leading to the formation of C2-monoarylated indoles. An effective Pd(0) carbene complex was successfully employed in the decarboxylative coupling of the heteroaromatic carboxylic acids (imidazo[1,2-a]pyridine and isoxazole) with aryl halides. For carboxyindoles, either decarboxylative coupling or tandem C?H arylation and decarboxylation occurred, leading to the formation of C2-monoarylated indoles.
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