Complete analyses of the proton and carbon chemical-shift assignments of D-mannurono-y-lactone (1) have been achieved by 1D and 2D NMR spectral measurements. At equilibrium, the anomeric LY and p forms were present in the ratio of 34:66 in D,O and 72:28 in Me,SO-d,. The solution data indicated tha
The composition and conformation of d-threo-3,4-hexodiulose in solution, and the X-ray crystal structure of its ββ anomer
✍ Scribed by Stephen J. Angyal; Donald C. Craig; János Kuszmann
- Publisher
- Elsevier Science
- Year
- 1989
- Tongue
- English
- Weight
- 534 KB
- Volume
- 194
- Category
- Article
- ISSN
- 0008-6215
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✦ Synopsis
The crystal structure of D-threo-3,Chexodiulose was determined, and it showed that the crystalline form is the p/3 anomer. In solution, the (~a anomer is preponderant, although all of its hydroxyl groups are cis to each other. In the crystal, the diulose assumes the endo,exo conformation; in the aqueous solutions of both anomers, the endo,endo form preponderates, whereas the acetates in chloroform are mainly in the exo,exo conformation. *Dedicated to the memory of Professor Edgar Lederer.
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