Synthesis, mechanism of formation and spatial arrangement of (2S,3S,6R)-2,6-diphenyl-3,4-dimethyl-6-ol
| dc.contributor.author | Nurkenov, O. A. | |
| dc.contributor.author | Fazylov, S. D. | |
| dc.contributor.author | Abulyaissova, L. K. | |
| dc.contributor.author | Turdybekov, K. M. | |
| dc.contributor.author | Shaltakov, S. N. | |
| dc.contributor.author | Isaeva, A. Zh. | |
| dc.date.accessioned | 2018-01-22T10:21:39Z | |
| dc.date.available | 2018-01-22T10:21:39Z | |
| dc.date.issued | 2013-12 | |
| dc.description.abstract | 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. | ru_RU |
| dc.identifier.citation | Synthesis, mechanism of formation and spatial arrangement of (2S,3S,6R)-2,6-diphenyl-3,4-dimethyl-6-ol/O. A. Nurkenov[a.o.]//Russian Journal of General Chemistry.-2013.-№12(83).- pp 2276–2280 | ru_RU |
| dc.identifier.issn | 1070-3632 | |
| dc.identifier.uri | https://rep.buketov.edu.kz/handle/data/2080 | |
| dc.language.iso | en | ru_RU |
| dc.publisher | Springer US | ru_RU |
| dc.relation.ispartofseries | Russian Journal of General Chemistry;№12(83) | |
| dc.title | Synthesis, mechanism of formation and spatial arrangement of (2S,3S,6R)-2,6-diphenyl-3,4-dimethyl-6-ol | ru_RU |
| dc.type | Article | ru_RU |