Journal
JOURNAL OF ORGANIC CHEMISTRY
Volume 65, Issue 14, Pages 4397-4408Publisher
AMER CHEMICAL SOC
DOI: 10.1021/jo000341v
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- NCI NIH HHS [CA-55268] Funding Source: Medline
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The oxidative cyclization of a phenolic amide to a spirolactam has long been regarded as an impossible reaction, because exposure of the substrates to a variety of oxidants results in formation of spirolactones with consequent loss of the amine segment. We recently communicated that this heretofore unknown transformation may be achieved by oxidation of oxazoline analogues of phenolic and indolic amides. Herein, we provide full details of our work.
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