DILACTONE FORMATION BY CHROMIC ANHYDRIDE OXIDATION OF THE GERMACRANOLIDE STIZOLICIN

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dc.contributor.author Suleimenov, E. M.
dc.contributor.author Raldugin, V. A.
dc.contributor.author Shakirov, M. M.
dc.contributor.author Adekenov, S. M.
dc.date.accessioned 2014-07-03T04:37:21Z
dc.date.available 2014-07-03T04:37:21Z
dc.date.issued 2014-07-03
dc.identifier.uri http://repository.enu.kz:8080/handle/data/11801
dc.description http://www.enu.kz ru_RU
dc.description.abstract The sidechain of the germacranolide stizolicin was oxidized by CrO3 in Py to form a lactone. The structure of the product was established as 4,5α-epoxy-7α,5,6,8β(H)-germacr-1(10),11(13)-dien-8α(3′-oxo-2′,5′-dihydrofuran-3′-carboxylyl)-12,6-olide using spectral data. ru_RU
dc.language.iso en ru_RU
dc.relation.ispartofseries UDC;547.314
dc.subject stizolicin, oxidation, dilactone, two-dimensional NMR ru_RU
dc.title DILACTONE FORMATION BY CHROMIC ANHYDRIDE OXIDATION OF THE GERMACRANOLIDE STIZOLICIN ru_RU
dc.type Article ru_RU


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