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3 citations found for Ayers, B.
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X-ray crystallography firmly established the relative stereochemistry of the title compound, C17H22N2O3. The absolute configuration was determined by use of 2-C-methyl-D-ribonolactone as the starting material. The compound exists as O—H
N hydrogen-bonded chains of molecules running parallel to the a-axis.
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X-ray crystallography firmly established the relative stereochemistry of the title compound, C16H20N2O3. The acetonide ring adopts an envelope conformation with one of the O atoms as the flap and the piperidine ring adopts a slightly twisted boat conformation. The absolute configuration was determined by use of D-ribose as the starting material. The compound exists as O—H
O hydrogen-bonded chains of molecules running parallel to the b axis.
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