Determination of Molecular Structure Using Vibrational Circular Dichroism Spectroscopy:  The Keto-lactone Product of Baeyer−Villiger Oxidation of (+)-(1R,5S)-Bicyclo[3.3.1]nonane-2,7-dione

2005 ◽  
Vol 70 (10) ◽  
pp. 3903-3913 ◽  
Author(s):  
P. J. Stephens ◽  
D. M. McCann ◽  
F. J. Devlin ◽  
T. C. Flood ◽  
E. Butkus ◽  
...  
1990 ◽  
Vol 44 (2) ◽  
pp. 235-238 ◽  
Author(s):  
Kevin M. Spencer ◽  
Steven J. Cianciosi ◽  
John E. Baldwin ◽  
Teresa B. Freedman ◽  
Laurence A. Nafie

2009 ◽  
Vol 4 (8) ◽  
pp. 1934578X0900400 ◽  
Author(s):  
Marcelo A. Muñoz ◽  
Carlos Areche ◽  
Aurelio San-Martín ◽  
Juana Rovirosa ◽  
Pedro Joseph-Nathan

The absolute configuration of the pentacyclic ichthyotoxin stypotriol, a constituent of Stypopodium zonale, was deduced to be 3S,5R,8R,9R,10S,13S,14S-(-)-1 by vibrational circular dichroism spectroscopy of the derived triacetate 2 in comparison to DFT B3LYP/DGDZVP calculations. Compound 2, C33H46O7 having 300 electrons, is the largest natural product successfully studied by VCD to date.


Sign in / Sign up

Export Citation Format

Share Document