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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Rahn, Thomas | - |
dc.contributor.author | Langer, Peter | - |
dc.date.accessioned | 2021-08-11T08:08:09Z | - |
dc.date.available | 2021-08-11T08:08:09Z | - |
dc.date.issued | 2021 | - |
dc.identifier.issn | 2525-2321 | - |
dc.identifier.uri | https://dspace.ctu.edu.vn/jspui/handle/123456789/61022 | - |
dc.description.abstract | A 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.iso | vi | vi_VN |
dc.relation.ispartofseries | Vietnam Journay of Chemistry;No.59(1) .- P.87-89 | - |
dc.subject | Butenolides | vi_VN |
dc.subject | Cyclization | vi_VN |
dc.subject | Cyclopropanes | vi_VN |
dc.subject | Heterocycles | vi_VN |
dc.subject | Regioselectivity | vi_VN |
dc.title | Synthesis and Reactions of 1 -cyclopropyl-1,3-bis(trimethylsilyloxy)-1,3-buatdiene | vi_VN |
dc.type | Article | vi_VN |
Appears in Collections: | Vietnam Journal of Chemistry |
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