Saborit Villarroya, GiselaCativiela, CarlosJimenez, Ana I.Bonjoch i Sesé, JosepBradshaw, Ben2019-02-132019-02-132018-10-091860-5397https://hdl.handle.net/2445/128207A straightforward synthetic entry to functionalized hydrindane compounds based on a rapid assembly of the core nucleus by a Danheiser cycloaddition is reported. Valuable bicyclic building blocks containing the fused five and six-membered carbocyclic ring system can be achieved in only four steps from a simple acyclic β-keto ester. Keywords: alkaloid; Danheiser annulation; decahydroquinoline5 p.application/pdfengcc-by (c) Saborit Villarroya, Gisela et al., 2018http://creativecommons.org/licenses/by/3.0/esCiclització (Química)AlcaloidesSíntesi orgànicaRing formation (Chemistry)AlkaloidsOrganic synthesisSynthesis of cis-hydrindan-2,4-diones bearing an all.carbon quaternary center by a Danheiser annulationinfo:eu-repo/semantics/article6832252019-02-13info:eu-repo/semantics/openAccess30410621