Ontology highlight
ABSTRACT:
SUBMITTER: Casas-Hinestroza JL
PROVIDER: S-EPMC7287697 | biostudies-literature | 2020 May
REPOSITORIES: biostudies-literature
Molecules (Basel, Switzerland) 20200512 10
The synthesis of phenyl-resorcinarenes and pyrogallolarenes is known to produce a conformational mixture of cone and chair isomers. Depending on the synthesis conditions the composition of the conformational mixture is variable; however, the cone conformer is the greatest proportion of phenyl-resorcin[4]arenes and chair conformer of pyrogallol[4]arenes. The experimental evidence suggests that phenyl-substituted resorcinarene and pyrogallolarene exist as a dynamic boat in solution. ...[more]