Journal
ORGANIC LETTERS
Volume 13, Issue 15, Pages 4136-4139Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol2016803
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Funding
- National Science Foundation
- National Institutes of Health Kansas University Center of Excellence in Chemical Methodology and Library Development [P50 GM069663]
- Division Of Chemistry
- Direct For Mathematical & Physical Scien [0946687] Funding Source: National Science Foundation
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A novel, efficient route to biologically and pharmaceutically Important o-(dimethylamino)aryl ketones and acridones has been developed starting from readily available 1,1-dimethylhydrazones of aldehydes and o-(trimethylsilyl)aryl triflates. The reaction proceeds under mild conditions, tolerates a wide range of functional groups, and provides the final products in good to excellent yields.
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