Absolute Configuration of the Meroditerpenoids Taondiol and Epitaondiol Diacetates by Vibrational Circular Dichroism

Heterocycles ◽  
2012 ◽  
Vol 85 (8) ◽  
pp. 1961 ◽  
Author(s):  
Pedro Joseph-Nathan ◽  
Marcelo A. Muñoz ◽  
Carlos Areche ◽  
Juana Rovirosa ◽  
Aurelio San Martín ◽  
...  
Heterocycles ◽  
2010 ◽  
Vol 81 (3) ◽  
pp. 625 ◽  
Author(s):  
Pedro Joseph-Nathan ◽  
Marcelo A. Muñoz ◽  
Carlos Areche ◽  
Juana Rovirosa ◽  
Aurelio San-Martín

2019 ◽  
Vol 14 (5) ◽  
pp. 1934578X1984979
Author(s):  
Alfredo R. Ortega ◽  
Nury Pérez-Hernández ◽  
Pedro Joseph-Nathan

The bark of the roots of Piscidia carthagenensis afforded the known insecticides rotenone (1) and millettone (2), as well as the new rotenoid piscicartone (3). The structure of 3 followed from nuclear magnetic resonance studies, while its absolute configuration (AC) was determined by vibrational circular dichroism (VCD) measurements in comparison with discrete Fourier transform B3LYP/DGDZVPcalculated spectra using the Compare VOA software. In addition, the AC of 1 and 2 was verified using the same VCD methodology.


2007 ◽  
Vol 70 (7) ◽  
pp. 1167-1172 ◽  
Author(s):  
Carlos M. Cerda-García-Rojas ◽  
Hugo A. García-Gutiérrez ◽  
Juan D. Hernández-Hernández ◽  
Luisa U. Román-Marín ◽  
Pedro Joseph-Nathan

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