Bulletin of the Chemical Society of Japan · 1992 · 10 citations · 12 references
Natural SciencesChemistryComputational ChemistryMolecular PhysicsOrganic ChemistryHeterocycle SynthesisOrganic SynthesisRetrosynthetic AnalysisDynamic Nmr Spectroscopy
Abstract Triptycene derivatives that carry C4-olefinic substituents at the 9-position, in which the olefin is connected to C(9) through an sp2 carbon, are synthesized. Their dynamic behaviors, as observed by dynamic NMR technique, are discussed on the basis of the results of MM2 calculations. The barrier to rotation of the olefinic groups is higher when there is a methyl group which directs inside relative to the triptycene skeleton, than the cases where no such a methyl group exists.
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Molecular Structure of Propylene
David R. Lide, Daniel Mølager Christensen · The Journal of Chemical Physics · 1961 · 227 citations
RECENT ADVANCES IN ATROPISOMERISM
Oki M · Topics in stereochemistry · 1983 · 191 citations