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The title compound 2 was synthesized by the reaction of 3-keto-D-xylose with O-C6H4NH2NH2 and characterized by IR, NMR and HRMS, and its crystal structure was determined by X-ray diffraction analysis. The crystal is of orthorhombic system (C21H22N2O5, Mr = 382.41), space group P212121 with a = 10.140(2), b = 10.802(2), c = 17.840(4) , β = 90°, V = 1954.1(7) 3, Z = 4, Dc = 1.300 g/cm3, F(000) = 808, μ = 0.094 mm-1, the final R = 0.0354 and wR = 0.0514 for 1924 observed reflections (I > 2σ(I)). One intermolecular and one intramolecular hydrogen bonds were found. The absolute configuration of this molecule was confirmed by comparison with that of the original material.
The title compound 2 was synthesized by the reaction of 3-keto-D-xylose with O-C6H4NH2NH2 and characterized by IR, NMR and HRMS, and its crystal structure was determined by X-ray diffraction analysis. The crystal is of orthorhombic system C21H22N2O5, Mr = 382.41), space group P212121 with a = 10.140 (2), b = 10.802 (2) and c = 17.840 (4) , Dc = 1.300 g / cm3, F (000) = 808, μ = 0.094 mm-1, the final R = 0.0354 and wR = 0.0514 for 1924 observed reflections (I> 2σ (I)). One intermolecular and one intramolecular hydrogen The absolute configuration of this molecule was confirmed by comparison with that of the original material.