Annulative ??-extension chemistry provides a concise synthetic route to polycyclic arenes. Herein, we disclose a nondirected annulation approach of unactivated simple arenes. The palladium-catalyzed 2-fold C???H arylation event facilitates tandem C???C linkage relays to furnish fully benzenoid triphenylene frameworks using cyclic diaryliodonium salts. The inseparable regioisomeric mixture of 1- and 2-methyltriphenylenes is identified by the combined analysis of ion mobility-mass spectrometry, gas-phase infrared spectroscopy, and molecular simulation studies
C–H activation of functionally rich molecules without the need for directing groups promises shorter...
C–H arylation of arenes without the use of directing groups is a challenge, even for simple molecule...
[[abstract]]Highly substituted triphenylene derivatives were prepared in good yields via the palladi...
Annulative π-extension chemistry provides aconcise synthetic route to polycyclic arenes. Herein, we ...
C–H activation can offer an efficient synthetic route to access graphene segments or polyc...
C-H activation is a versatile tool for appending aryl groups to aromatic systems. However, heavy dem...
C−H activation is a versatile tool for appending aryl groups to aromatic systems. However, heavy dem...
A novel ligand-free Pd-catalyzed cascade reaction between <i>o-</i>chlorobenzoic acids and cyclic di...
Due to their ubiquity in nature and frequent use in organic electronic materials, benzothiophenes ar...
After a decade of research, developing one-step synthetic methods for selective C-H arylation is sti...
The palladium catalyzed synthesis of 14-phenylbenzo[f]tetraphene-9-carbonitrile derivatives as cor...
Aromatic compounds represent one of the most abundant classes of organic molecules, and are suitable...
A ZnBr<sub>2</sub>-mediated regioselective annulation of unsymmetrical 1,2-diarylmethinedipivalates ...
Under palladium-catalysis, norbornene 1, dicyclopentadiene 10, norbornenol 13, and norbornenone 15 r...
Owing to the synthetic importance of branched olefinated products, we report palladium catalyzed for...
C–H activation of functionally rich molecules without the need for directing groups promises shorter...
C–H arylation of arenes without the use of directing groups is a challenge, even for simple molecule...
[[abstract]]Highly substituted triphenylene derivatives were prepared in good yields via the palladi...
Annulative π-extension chemistry provides aconcise synthetic route to polycyclic arenes. Herein, we ...
C&#8211;H activation can offer an efficient synthetic route to access graphene segments or polyc...
C-H activation is a versatile tool for appending aryl groups to aromatic systems. However, heavy dem...
C−H activation is a versatile tool for appending aryl groups to aromatic systems. However, heavy dem...
A novel ligand-free Pd-catalyzed cascade reaction between <i>o-</i>chlorobenzoic acids and cyclic di...
Due to their ubiquity in nature and frequent use in organic electronic materials, benzothiophenes ar...
After a decade of research, developing one-step synthetic methods for selective C-H arylation is sti...
The palladium catalyzed synthesis of 14-phenylbenzo[f]tetraphene-9-carbonitrile derivatives as cor...
Aromatic compounds represent one of the most abundant classes of organic molecules, and are suitable...
A ZnBr<sub>2</sub>-mediated regioselective annulation of unsymmetrical 1,2-diarylmethinedipivalates ...
Under palladium-catalysis, norbornene 1, dicyclopentadiene 10, norbornenol 13, and norbornenone 15 r...
Owing to the synthetic importance of branched olefinated products, we report palladium catalyzed for...
C–H activation of functionally rich molecules without the need for directing groups promises shorter...
C–H arylation of arenes without the use of directing groups is a challenge, even for simple molecule...
[[abstract]]Highly substituted triphenylene derivatives were prepared in good yields via the palladi...