Journal
JOURNAL OF ORGANIC CHEMISTRY
Volume 81, Issue 22, Pages 10641-10650Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.6b02481
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- GlaxoSmithKline
- EPSRC
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A Rh-catalyzed ortho-amidation of 2-aryloxazo-lines offers an efficient and direct route to a range of sulfonamides. The scope of the reaction is very broad with respect to sulfonamide substrate, but the position and electronic nature of the substituents on the aryl moiety of the oxazoline lead to a surprising modulation of reactivity. The reactivity of sulfonamides in comparison to trifluoroacetamide is compared, the latter undergoing Rh-catalyzed amidation more rapidly.
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