Synthesis, mechanism of formation and spatial arrangement of (2S,3S,6R)-2,6-diphenyl-3,4-dimethyl-6-ol

Alkylation of alkaloid D-pseudoephedrine with bromoacetophenone results in a morpholine derivative. Structural and energy characteristics of the molecules of the starting, intermediate, and final reaction products were calculated by ab initio method in the HF/6-31G(d,p) approximation. The spatial st...

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Veröffentlicht in:Russian journal of general chemistry 2013-12, Vol.83 (12), p.2276-2280
Hauptverfasser: Nurkenov, O. A., Fazylov, S. D., Abulyaissova, L. K., Turdybekov, K. M., Shaltakov, S. N., Isaeva, A. Zh
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Sprache:eng
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Zusammenfassung:Alkylation of alkaloid D-pseudoephedrine with bromoacetophenone results in a morpholine derivative. Structural and energy characteristics of the molecules of the starting, intermediate, and final reaction products were calculated by ab initio method in the HF/6-31G(d,p) approximation. The spatial structure of the final reaction product was determined by X-ray diffraction analysis.
ISSN:1070-3632
1608-3350
DOI:10.1134/S1070363213120098