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• W2893457943 endingPage "1928" @default.
• W2893457943 startingPage "1924" @default.
• W2893457943 abstract "A one-pot, regiospecific synthesis of dihydrofurans bearing a quaternary centre and tetrasubstituted furans is developed from the formal [3 + 2] annulation of tert-propargyl alcohols and 1,3-diketones under Ca(ii)/DBU conditions. The reaction proceeds through the SN2I mechanism to form homoallenyl ketone and a subsequent cycloisomerization to yield novel and new chemical entities of privileged scaffolds." @default.
• W2893457943 created "2018-10-05" @default.
• W2893457943 creator A5000987714 @default.
• W2893457943 creator A5067722040 @default.
• W2893457943 date "2019-01-01" @default.
• W2893457943 modified "2023-10-14" @default.
• W2893457943 title "Regiospecific formal [3 + 2] annulation of<i>tert</i>-propargyl alcohols with acyclic 1,3-diketones<i>via</i>the cycloisomerization of homoallenyl ketones" @default.
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• W2893457943 doi "https://doi.org/10.1039/c8ob02158a" @default.
• W2893457943 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30283958" @default.
• W2893457943 hasPublicationYear "2019" @default.
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