Synthesis of Thiapillar [6] arenes Bearing Redox-Active (Hydro) quinone Groups. Electrochemical and XRD Study

N Nikishkin, J Cějka, V Eigner… - The Journal of …, 2023 - ACS Publications
Pillar [n] arenes are among the newest members of the macrocyclic family. Nevertheless,
their conformational behavior and binding properties as well as redox properties of …

Silapillar[n]arenes: Their Enhanced Electronic Conjugation and Conformational Versatility

S Ohtani, S Akine, K Kato, S Fa, T Shi… - Journal of the American …, 2024 - ACS Publications
During recent decades, methylene-bridged macrocyclic arenes have been widely used in
supramolecular chemistry. However, their π-conjugations are very weak, as the methylene …

Thiapillar [5] arenes: Structures, Properties, and Host-Guest chemistry

J Xie, W Wang, Z Xi, X Zhang, Z Yang, H Yuan, M He - Chemical Physics, 2024 - Elsevier
The chemical modification of bridging groups of the pillar [n] arenes is an important way to
functional derivatization and expand the application fields. So far, however, there have been …

Rapid Access to Chiral and Tripodal Cavitands from β‐Pinene

X Wang, RZ Pavlović, TJ Finnegan… - … A European Journal, 2022 - Wiley Online Library
We report Pd‐catalyzed cyclotrimerization of (+)‐α‐bromoenone, obtained from
monoterpene β‐pinene, into an enantiopure cyclotrimer. This C3 symmetric compound has …