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NMR analysis and crystal structure of hydroxyclerodanes from Mexican Salvia species
Alfredo Ortega
NAYTZE DALIA ORTIZ PASTRANA
BRENDA YUDITH BEDOLLA GARCIA
Rubén A. Toscano
FRANCISCO ELIHU BAUTISTA REDONDA
En Embargo
31-08-2019
Atribución-NoComercial-SinDerivadas
https://doi.org/10.1016/j.molstruc.2017.03.091
Clerodane diterpenes
Hydroxyclerodanes
Salvia species
NMR analysis
X-ray diffraction
Crystal structure
"NMR and single crystal X-ray diffraction analysis of seven clerodanes from Mexican Salvia species was performed. We focused on clerodanes with tertiary hydroxyl group at C-4, C-8, and C-10, in which the establishment of absolute configuration around these chiral centers is nontrivial and the 13C NMR signals can be misassigned. In addition, the analysis by 1H NMR in aprotic solvent allowed us to establish a common pattern that correlates the chemical shift with the position of the hydroxyl groups, which constitute a good methodology for future structural elucidation of these kinds of compounds. The obtained data allowed us to establish the absolute configuration of five of these diterpenes and the structural revision of salvimicrophyllin D (7)."
Elsevier
2017
Artículo
Alfredo Ortega, Naytzé Ortiz-Pastrana, Brenda Y. Bedolla-García, Rubén A. Toscano, Elihú Bautista, NMR analysis and crystal structure of hydroxyclerodanes from Mexican Salvia species, Journal of Molecular Structure, Volume 1141, 2017, Pages 157-162.
QUÍMICA
Versión aceptada
acceptedVersion - Versión aceptada
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