Characterization of a carboxyl-terminated butadiene-acrylonitrile copolymer by two-dimensional nuclear magnetic resonance

1990 ◽  
Vol 23 (8) ◽  
pp. 2145-2152 ◽  
Author(s):  
Treliant Fang
1987 ◽  
Vol 65 (11) ◽  
pp. 2519-2525 ◽  
Author(s):  
Stewart McLean ◽  
Marion Perpick-Dumont ◽  
William F. Reynolds ◽  
Helen Jacobs ◽  
Sagar Singh Lachmansing

It is shown that 1H–13C shift-correlated two-dimensional spectra obtained for polarization transfer via two-bond and three-bond 13C–1H coupling can, in conjunction with related experiments, be used to assign unambiguously the molecular skeletons of two of the less common triterpenes, moretenone and 3-acetylaleuritolic acid. It is concluded that this is a technique of considerable generality for assigning structures of triterpenes and is more reliable than alternative approaches such as mass spectral fragmentation patterns. It has the additional benefit of simultaneously providing reliable 13C and 1H spectral assignments for these compounds.


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