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Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/128207
Synthesis of cis-hydrindan-2,4-diones bearing an all.carbon quaternary center by a Danheiser annulation
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Abstract
A 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; decahydroquinoline
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SABORIT VILLARROYA, Gisela, et al. Synthesis of cis-hydrindan-2,4-diones bearing an all.carbon quaternary center by a Danheiser annulation. Beilstein Journal of Organic Chemistry. 2018. Vol. 14, num. 2597-2601. ISSN 1860-5397. [consulted: 16 of June of 2026]. Available at: https://hdl.handle.net/2445/128207