The relative configuration at C-2 of 2,4-dimethyl-3,4-O-isopropyl-idene-l- arabinono lactone, C10H16O5, which exists in the boat form, was unequivocally established by X-ray crystallographic analysis. The absolute configuration was determined by the use of 2-C-methyl-d-ribonolactone as a starting material. © 2007 International Union of Crystallography
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 ...
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 ...
The relative configuration at C-2 of the title lactone, C14H22O6, which exists in the five-membered ...
The relative configuration at position C-2 of the title lactone, C11H18O6, which exists in the five-...
The relative configuration at position C-2 of the title lactone, C11H18O6, which exists in the five-...
The relative configuration at position C-2 of the title lactone, C11H18O6, which exists in the five-...
The relative configuration of the title compound, C11H18O6, was firmly established by X-ray crystall...
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, C10H16O4, was firmly established by X-ray crystall...
The relative configuration of the title compound, C8H 12O5, was unequivocally established by X-ray c...
The relative configuration of the title compound, C8H 12O5, was unequivocally established by X-ray c...
The relative configuration of the title compound, C9H14NO5, formed by catalytic hydrogenation of an ...
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 ...
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 ...
The relative configuration at C-2 of the title lactone, C14H22O6, which exists in the five-membered ...
The relative configuration at position C-2 of the title lactone, C11H18O6, which exists in the five-...
The relative configuration at position C-2 of the title lactone, C11H18O6, which exists in the five-...
The relative configuration at position C-2 of the title lactone, C11H18O6, which exists in the five-...
The relative configuration of the title compound, C11H18O6, was firmly established by X-ray crystall...
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, C10H16O4, was firmly established by X-ray crystall...
The relative configuration of the title compound, C8H 12O5, was unequivocally established by X-ray c...
The relative configuration of the title compound, C8H 12O5, was unequivocally established by X-ray c...
The relative configuration of the title compound, C9H14NO5, formed by catalytic hydrogenation of an ...
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 ...
In the title compound, C15H16O6, obtained from the acylation reaction between 2,3-O-isopropylidene-d...