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

dc.contributor.authorNurkenov, O. A.
dc.contributor.authorFazylov, S. D.
dc.contributor.authorAbulyaissova, L. K.
dc.contributor.authorTurdybekov, K. M.
dc.contributor.authorShaltakov, S. N.
dc.contributor.authorIsaeva, A. Zh.
dc.date.accessioned2018-06-08T06:38:40Z
dc.date.available2018-06-08T06:38:40Z
dc.date.issued2013-12
dc.description.abstractAlkylation 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.citationSynthesis, 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.-2276-2280ru_RU
dc.identifier.urihttps://rep.buketov.edu.kz/handle/data/3136
dc.language.isoenru_RU
dc.publisherSpringerru_RU
dc.relation.ispartofseriesRussian Journal of General Chemistry;№12(83)
dc.titleSynthesis, mechanism of formation and spatial arrangement of (2S,3S,6R)-2,6-diphenyl-3,4-dimethyl-6-olru_RU
dc.typeArticleru_RU

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