Synthesis of fused N-heterocycles via tandem C-H activation
Research output: Contribution to journal › Article
Colleges, School and Institutes
The synthesis of fused N-heterocycles has been developed using an intramolecular cyclisation of purines or benzimidazoles. A range of medium and large rings were prepared. © 2012 The Royal Society of Chemistry.
|Number of pages||3|
|Publication status||Published - 7 Oct 2012|