Unexpected Phenyl Group Rearrangement during an Intramolecular Scholl Reaction Leading to an Alkoxy-Substituted Hexa-peri-hexabenzocoronene
Organic Letters2007Vol. 9(13), pp. 2485–2488
Citations Over TimeTop 12% of 2007 papers
Abstract
A simple dimethoxy-substituted hexa-peri-hexabenzocoronene (m-dimethoxy HBC) was unexpectedly obtained along with a bis-spirocyclic dienone during an intramolecular Scholl reaction of its para isomer.
Related Papers
- → Intramolecular isotope effects in the reactions of CF32+ and CO22+ with HD(2001)28 cited
- → Nature of weak inter-and intramolecular interactions in crystals 8. Influence of intermolecular contacts on the strength of intramolecular O-H...N bonds in crystals of 3-(2-hydroxyphenyl)-1,2,4-triazoles(2006)3 cited
- → Stimulation intramolecular F⋯H hydrogen bond by intramolecular N → Si interaction in Si-fluoro derivatives of 8-mercaptoquinoline: DFT and MP2 calculations(2018)1 cited
- Conformations and Intramolecular Hydrogen Bonds of a Series of Amino-alcohols(2013)
- Susquehanna Chorale Spring Concert "Roots and Wings"(2017)