Please use this identifier to cite or link to this item: https://dspace.ctu.edu.vn/jspui/handle/123456789/61022
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dc.contributor.authorRahn, Thomas-
dc.contributor.authorLanger, Peter-
dc.date.accessioned2021-08-11T08:08:09Z-
dc.date.available2021-08-11T08:08:09Z-
dc.date.issued2021-
dc.identifier.issn2525-2321-
dc.identifier.urihttps://dspace.ctu.edu.vn/jspui/handle/123456789/61022-
dc.description.abstractA cyclopropyl-substituted 1,3-bis(silyl enol ether) was prepared in two steps and subsequently employed in the cyclization with oxalyl chloride to give a cyclopropyl-carbonyl substituted ᵧ-alkylidenebutenolide. The cyclization of the 1,3-bis(silyl enol ether) with 1,3-dielectrophiles afforded cyclopropyl-carbonyl substituted phenols. The reactions proceeded with very good regioselectivity.vi_VN
dc.language.isovivi_VN
dc.relation.ispartofseriesVietnam Journay of Chemistry;No.59(1) .- P.87-89-
dc.subjectButenolidesvi_VN
dc.subjectCyclizationvi_VN
dc.subjectCyclopropanesvi_VN
dc.subjectHeterocyclesvi_VN
dc.subjectRegioselectivityvi_VN
dc.titleSynthesis and Reactions of 1 -cyclopropyl-1,3-bis(trimethylsilyloxy)-1,3-buatdienevi_VN
dc.typeArticlevi_VN
Appears in Collections:Vietnam Journal of Chemistry

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