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An aminobenzannulation reaction of propargylic ester and isocyanide to access multi-functionalized aryl amine derivatives

An aminobenzannulation of two molecular isocyanides and propargylic ester has been reported. This reaction involves sequential annulation and rearrangement processes, providing an efficient access to the multi-substituted aniline and naphthylamine... Click to show full abstract

An aminobenzannulation of two molecular isocyanides and propargylic ester has been reported. This reaction involves sequential annulation and rearrangement processes, providing an efficient access to the multi-substituted aniline and naphthylamine...

Keywords: propargylic ester; aminobenzannulation reaction; access multi

Journal Title: Organic Chemistry Frontiers
Year Published: 2024

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