Cargando…
Synthesis and Stereochemical Characterization of a Novel Chiral α-Tetrazole Binaphthylazepine Organocatalyst
A novel α-tetrazole-substituted 1,1′-binaphthylazepine chiral catalyst has been synthesized and its absolute configuration has been determined by DFT computational analysis of the vibrational circular dichroism (VCD) spectrum of its precursor. The VCD analysis, carried out through the model averagin...
Autores principales: | Summa, Assunta, Scafato, Patrizia, Belviso, Sandra, Monaco, Guglielmo, Zanasi, Riccardo, Longhi, Giovanna, Abbate, Sergio, Superchi, Stefano |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9413694/ https://www.ncbi.nlm.nih.gov/pubmed/36014353 http://dx.doi.org/10.3390/molecules27165113 |
Ejemplares similares
-
Absolute Configuration Assignment to Chiral Natural
Products by Biphenyl Chiroptical Probes: The Case of the Phytotoxins
Colletochlorin A and Agropyrenol
por: Santoro, Ernesto, et al.
Publicado: (2020) -
Electronic Currents Induced by Optical Fields and Rotatory Power Density in Chiral Molecules
por: Summa, Francesco Ferdinando, et al.
Publicado: (2021) -
Regio- and stereoselective intermolecular carbolithiation reactions
por: Marsico, G., et al.
Publicado: (2020) -
Computational Approaches and Use of Chiroptical Probes in the Absolute Configuration Assignment to Natural Products by ECD Spectroscopy: A 1,2,3-Trihydroxy-p-menthane as a Case Study
por: Marsico, Giulia, et al.
Publicado: (2022) -
Magnetic Characterization of the Infinitene Molecule
por: Monaco, Guglielmo, et al.
Publicado: (2022)