Glycidol esters from diethylamido-(4-phenylthiazolyl-2-amido)-ketophosphonates and their chemical modification

dc.contributor.authorSal’keeva, L. K.
dc.contributor.authorMinayeva, E. V.
dc.contributor.authorNurmaganbetova, M. T.
dc.contributor.authorKokzhalova, B. Z.
dc.contributor.authorMantel’, A. I.
dc.date.accessioned2018-06-11T09:28:51Z
dc.date.available2018-06-11T09:28:51Z
dc.date.issued2009-04
dc.description.abstractThiazolyl-containing esters of alpha-ketophosphonic acids (KPE) unknown earlier were synthesized and investigated in Darzens-Claisen reaction. Reactions were demonstrated to proceed by a classic scheme to form the corresponding phosphorylated glycidol esters whose alkaline hydrolysis gave rise to phosphorylated aldehydes of interesting nature.ru_RU
dc.identifier.citationGlycidol esters from diethylamido-(4-phenylthiazolyl-2-amido)-ketophosphonates and their chemical modification\L. K. Sal’keeva[a.o.]\\Russian Journal of General Chemistry.-2009.-№4(79).-pp.-755-758ru_RU
dc.identifier.urihttps://rep.buketov.edu.kz/handle/data/3161
dc.language.isoenru_RU
dc.publisherSpringerru_RU
dc.relation.ispartofseriesRussian Journal of General Chemistry;№4(79)
dc.titleGlycidol esters from diethylamido-(4-phenylthiazolyl-2-amido)-ketophosphonates and their chemical modificationru_RU
dc.typeArticleru_RU

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