Determination of anomeric configuration of D-ribofuranosyl nucleosides from nuclear magnetic resonance spectra by a pattern recognition technique

1975 ◽  
Vol 47 (9) ◽  
pp. 1702-1703 ◽  
Author(s):  
Jure. Zupan ◽  
Joze. Kobe ◽  
Dusan. Hadzi
1967 ◽  
Vol 45 (23) ◽  
pp. 2969-2978 ◽  
Author(s):  
Wayland E. Noland ◽  
Bruce A. Langager ◽  
Joseph W. Manthey ◽  
Anthony G. Zacchei ◽  
Darryl L. Petrak ◽  
...  

The nuclear magnetic resonance spectra of representative 5-nitro-6-substituted-2-norbornenes (II–VII) are described. From the spectra, ratios of the two possible endo–exo trans stereoisomers derived from the Diels–Alder reaction of cyclopentadiene with the appropriate trans nitroölefin are estimated as shown in Table II. For all cases, there was predominance (3:1 to 9:1) of the 5-endo-nitro trans stereoisomer. The synthesis of the 6-(p-nitrophenyl) (V), 6-(2-furyl) (VI), and 6-(2-thienyl) (VII) derivatives is reported and the 6-ethyl derivative (III) has been characterized


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