Synthesis of fused N-heterocycles via tandem C-H activation

Ge Meng; Hong-Ying Niu; Gui-Rong Qu; John S Fossey; Jian-Ping Li; Hai-Ming Guo

doi:10.1039/c2cc34158a

Synthesis of fused N-heterocycles via tandem C-H activation

Chem Commun (Camb). 2012 Oct 7;48(77):9601-3. doi: 10.1039/c2cc34158a.

Authors

Ge Meng¹, Hong-Ying Niu, Gui-Rong Qu, John S Fossey, Jian-Ping Li, Hai-Ming Guo

Affiliation

¹ College of Chemistry and Environmental Science, Key Laboratory of Green Chemical Media and Reactions of Ministry of Education, Henan Normal University, Xinxiang 453007, Henan, China.

PMID: 22892833
DOI: 10.1039/c2cc34158a

Abstract

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.

Publication types

Research Support, Non-U.S. Gov't

MeSH terms

Benzimidazoles / chemistry*
Cyclization
Heterocyclic Compounds / chemical synthesis*
Heterocyclic Compounds / chemistry
Molecular Structure
Purines / chemistry*
Stereoisomerism

Substances

Benzimidazoles
Heterocyclic Compounds
Purines