The crystal structure of the title compound, C(13)H(14)O(5), establishes (i) the (S) - rather than (R) - configuration at the acetal carbon and (ii) that both the acetal and the lactone form five- rather than six-membered rings; the absolute configuration is determined by the use of 2-C-methyl-d-ribono-1,4-lactone as the starting material. The compound consists of hydrogen-bonded chains of mol-ecules running along the a axis; there are no unusual packing features. Only classical hydrogen bonding has been considered
X-ray crystallography unequivocally shows that protection of the free hydroxyl group of 3,5-O-benzyl...
X-ray crystallography unequivocally shows that protection of the free hydroxyl group of 3,5-O-benzyl...
The relative configuration of the title compound, C10H16O6, was firmly established by X-ray crystall...
The relative configuration of the title compound, C11H18O6, was firmly established by X-ray crystall...
The relative configuration of the title compound, C11H18O6, was firmly established by X-ray crystall...
The structures of both lactones derived from the Kiliani ascension of 2-C-methyl-D-threose were defi...
X-ray crystallography unequivocally confirmed the stereochemistry of the 2-C-methyl group in the tit...
The relative configuration and ring size of the title compound, C 7H12O6, were established by X-ray ...
The relative configuration of the title compound, C9H16O5, has been firmly established by X-ray crys...
The relative configuration of the title compound, C9H16O5, has been firmly established by X-ray crys...
In the title compound, C15H16O6, obtained from the acylation reaction between 2,3-O-isopropylidene-d...
The title compound (systematic name3,4-dihydr-oxy-3-phenyl-furan-2-one), C(10)H(10)O(4), features a ...
The relative configuration at C-2 of the title lactone, C14H22O6, which exists in the five-membered ...
In the title compound, C15H16O6, obtained from the acylation reaction between 2,3-O-isopropylidene-d...
The relative configuration at C-2 of the title lactone, C14H22O6, which exists in the five-membered ...
X-ray crystallography unequivocally shows that protection of the free hydroxyl group of 3,5-O-benzyl...
X-ray crystallography unequivocally shows that protection of the free hydroxyl group of 3,5-O-benzyl...
The relative configuration of the title compound, C10H16O6, was firmly established by X-ray crystall...
The relative configuration of the title compound, C11H18O6, was firmly established by X-ray crystall...
The relative configuration of the title compound, C11H18O6, was firmly established by X-ray crystall...
The structures of both lactones derived from the Kiliani ascension of 2-C-methyl-D-threose were defi...
X-ray crystallography unequivocally confirmed the stereochemistry of the 2-C-methyl group in the tit...
The relative configuration and ring size of the title compound, C 7H12O6, were established by X-ray ...
The relative configuration of the title compound, C9H16O5, has been firmly established by X-ray crys...
The relative configuration of the title compound, C9H16O5, has been firmly established by X-ray crys...
In the title compound, C15H16O6, obtained from the acylation reaction between 2,3-O-isopropylidene-d...
The title compound (systematic name3,4-dihydr-oxy-3-phenyl-furan-2-one), C(10)H(10)O(4), features a ...
The relative configuration at C-2 of the title lactone, C14H22O6, which exists in the five-membered ...
In the title compound, C15H16O6, obtained from the acylation reaction between 2,3-O-isopropylidene-d...
The relative configuration at C-2 of the title lactone, C14H22O6, which exists in the five-membered ...
X-ray crystallography unequivocally shows that protection of the free hydroxyl group of 3,5-O-benzyl...
X-ray crystallography unequivocally shows that protection of the free hydroxyl group of 3,5-O-benzyl...
The relative configuration of the title compound, C10H16O6, was firmly established by X-ray crystall...