A visible light-promoted C-H insertion between diazoamides and 1,3-diketones leads to the corresponding 3-substituted-2-oxindoles in good yield.
A visible light-promoted C-H insertion between diazoamides and 1,3-diketones leads to the corresponding 3-substituted-2-oxindoles in good yield. A subsequent reaction of the resulting product with hydrazine hydrate, followed by alkylation,...
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Muthusamy et al. (2026) studied this question.
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