scholarly journals Hydroxyl proton resonances of methyl 4,6-O-benzylidene-.ALPHA.-and -.BETA.-D-allopyranosides in dimethyl sulfoxide solution.

1977 ◽  
Vol 41 (5) ◽  
pp. 907-908 ◽  
Author(s):  
Yôtaro KONDO ◽  
Keisuke KITAMURA
1977 ◽  
Vol 55 (1) ◽  
pp. 141-144 ◽  
Author(s):  
Yôtaro Kondo ◽  
Keisuke Kitamura

Proton magnetic resonance spectra of methyl 4,6-O-benzylidene-α- and β-D-glucopyranosides (1 and 10) and their mono-substituted derivatives are determined in dimethyl sulfoxide solution. Assignments of the hydroxyl group resonances of 1 and 10 are confirmed by means of INDOR techniques. It is shown that the position of the hydroxyl substituent of the mono-substituted derivatives of 1 and 10 can be determined by using the coupling constants JH—C—O—H. It is proposed that the vicinal diols of 1 and 10 give 1:1 associations with dimethyl sulfoxide molecules, and the C—H and O—H bonds at position 2 of the mono-substituted derivatives of 1 are approximately anti.


1973 ◽  
Vol 41 (12) ◽  
pp. 880-883 ◽  
Author(s):  
Shuta NAKAGAWA ◽  
Zenichiro TAKEHARA ◽  
Shiro YOSHIZAWA

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