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

Sal’keeva, L. K.; Minayeva, E. V.; Nurmaganbetova, M. T.; Kokzhalova, B. Z.; Mantel, A. I.

dc.contributor.author	Sal’keeva, L. K.
dc.contributor.author	Minayeva, E. V.
dc.contributor.author	Nurmaganbetova, M. T.
dc.contributor.author	Kokzhalova, B. Z.
dc.contributor.author	Mantel, A. I.
dc.date.accessioned	2018-01-15T05:41:35Z
dc.date.available	2018-01-15T05:41:35Z
dc.date.issued	2009-04
dc.identifier.citation	Glycidol 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 755–758	ru_RU
dc.identifier.issn	1070-3632
dc.identifier.uri	http://rep.ksu.kz/handle/data/2017
dc.description.abstract	Thiazolyl-containing esters of α-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.language.iso	en	ru_RU
dc.publisher	SP MAIK Nauka/Interperiodica	ru_RU
dc.relation.ispartofseries	Russian Journal of General Chemistry;№4(79)
dc.title	Glycidol esters from diethylamido-(4-phenylthiazolyl-2-amido)-ketophosphonates and their chemical modification	ru_RU
dc.type	Article	ru_RU