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...
               
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