4.7 Article

5-Azadibenzo[a,g]corannulene

Journal

ORGANIC CHEMISTRY FRONTIERS
Volume 4, Issue 5, Pages 688-698

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c6qo00831c

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Funding

  1. National Science Foundation
  2. Department of Energy

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5-Azadibenzo[a,g] corannulene, the first azacorannulene with a nitrogen on the rim, has been synthesized in seven steps from 4-bromoisoquinoline. The strained pyridine ring opens thermally to a polycyclic aromatic nitrile and hydrolytically to an amino aldehyde with the same polycyclic aromatic hydrocarbon framework.

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