Determination of the signs of long-range proton spin coupling constants by nuclear magnetic triple resonance

1964 ◽  
Vol 7 (1) ◽  
pp. 45-56 ◽  
Author(s):  
A.D. Cohen ◽  
R. Freeman ◽  
K.A. McLauchlan ◽  
D.H. Whiffen
1969 ◽  
Vol 47 (9) ◽  
pp. 1507-1514 ◽  
Author(s):  
T. Schaefer ◽  
S. S. Danyluk ◽  
C. L. Bell

The signs of all proton–proton and proton–fluorine spin–spin coupling constants in 2-fluoro-3-methylpyridine have been determined by double and triple resonance experiments. The signs of the longrange coupling constants, JH,CH3 and JF,CH3 are the same as in fluorotoluene derivatives. Their magnitudes are consistent with the assumption that the nitrogen atom primarily polarizes the σ bonds in the molecule, leaving the π contribution to the long-range coupling relatively unaffected.


1999 ◽  
Vol 64 (3) ◽  
pp. 866-876 ◽  
Author(s):  
Nobuaki Matsumori ◽  
Daisuke Kaneno ◽  
Michio Murata ◽  
Hideshi Nakamura ◽  
Kazuo Tachibana

Author(s):  
Anwar, E. M. Noreljaleel

A new methods for elucidating stereochemistry of organic compounds was developed on the basis of long-range proton–carbon coupling constants (2,3JC,H) and interpreting spin-coupling constants (3JH,H). Reaction of compound containing pyrin ring with nucleophile reagent was done to open the ring. HSQC-TOCSY experiments one of the new NMR spectroscopy method used to measure this values of spin-coupling constants and elucidating the stereochemistry of the product.


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