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The development of novel directing groups is a valuable strategy to secure the advancement of catalytic C–H functionalization. To illustrate the feasibility of urazoles as heterocyclic directing groups, we herein present the ruthenium(II)-catalyzed annulation of N–H/C–H bonds on N -aryl urazoles with vinylene carbonate. This transformation provides the rapid construction of triazolocinnoline derivatives as hemiaminal and dehydrated forms. A series of mechanistic investigations and post-transformations highlighted the amenability of the developed method.
Kang et al. (Thu,) studied this question.