Regiospecific formal [3 + 2] annulation of: Tert -propargyl alcohols with acyclic 1,3-diketones via the cycloisomerization of homoallenyl ketones

dc.contributor.author Yaragorla, Srinivasarao
dc.contributor.author Rajesh, P.
dc.date.accessioned 2022-03-27T08:49:24Z
dc.date.available 2022-03-27T08:49:24Z
dc.date.issued 2019-01-01
dc.description.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 S N 2 I mechanism to form homoallenyl ketone and a subsequent cycloisomerization to yield novel and new chemical entities of privileged scaffolds.
dc.identifier.citation Organic and Biomolecular Chemistry. v.17(7)
dc.identifier.issn 14770520
dc.identifier.uri 10.1039/c8ob02158a
dc.identifier.uri http://xlink.rsc.org/?DOI=C8OB02158A
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/11872
dc.title Regiospecific formal [3 + 2] annulation of: Tert -propargyl alcohols with acyclic 1,3-diketones via the cycloisomerization of homoallenyl ketones
dc.type Journal. Article
dspace.entity.type
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