Please use this identifier to cite or link to this item: http://hdl.handle.net/2067/51037
Title: Diaryl-Pyrano-Chromenes Atropisomers: Stereodynamics and Conformational Studies
Authors: Ciogli, Alessia
Andrea Fochetti 
Sorato, Andrea
Fabrizi, Giancarlo
Matera, Nunzio
Mazzanti, Andrea
Mancinelli, Michele
Journal: MOLECULES 
Issue Date: 2023
Abstract: 
The dynamic scenario of di-aryls-pyrano-chromenes was investigated using DFT calculations. The symmetry of the chromene scaffold and the presence of two ortho-substituted aryls substituents can generate two syn/anti diastereoisomers and conformational enantiomers with different rotational barriers. The relative conformations and configurations were derived using NOESY-1D experiments. Depending on the energies related to the conformational exchange, the experimental energy barriers were determined through Dynamic NMR, Dynamic HPLC or kinetic studies. The atropisomeric pairs were resolved in the latter scenario, and their absolute configuration was assigned using the ECD/TD-DFT method.
URI: http://hdl.handle.net/2067/51037
ISSN: 1420-3049
DOI: 10.3390/molecules28134915
Appears in Collections:A1. Articolo in rivista

Files in This Item:
File Description SizeFormat Existing users please
2023 Atropoisomeri Molecules.pdf4.11 MBAdobe PDF    Request a copy
Show full item record

Page view(s)

2
checked on Apr 20, 2024

Google ScholarTM

Check

Altmetric


All documents in the "Unitus Open Access" community are published as open access.
All documents in the community "Prodotti della Ricerca" are restricted access unless otherwise indicated for specific documents