A commercially available rhodium(II) complex catalyzes the direct arylation of 5-diazobarbituric acids with arenes, allowing straightforward access to 5-aryl barbituric acids. Free N-H groups are tolerated on the barbituric acid, with no complications arising from N-H insertion processes. This method was applied to the concise synthesis of a potent matrix metalloproteinase (MMP) inhibitor.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4479025 | PMC |
http://dx.doi.org/10.1002/anie.201502324 | DOI Listing |
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