Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/128207
Title: Synthesis of cis-hydrindan-2,4-diones bearing an all.carbon quaternary center by a Danheiser annulation
Author: Saborit Villarroya, Gisela
Cativiela, Carlos
Jimenez, Ana I.
Bonjoch i Sesé, Josep
Bradshaw, Ben
Keywords: Ciclització (Química)
Alcaloides
Síntesi orgànica
Ring formation (Chemistry)
Alkaloids
Organic synthesis
Issue Date: 9-Oct-2018
Publisher: Beilstein Institute
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
Note: Reproducció del document publicat a: https://doi.org/10.3762/bjoc.14.237
It is part of: Beilstein Journal of Organic Chemistry, 2018, vol. 14, p. 2597-2601
Related resource: https://doi.org/10.3762/bjoc.14.237
URI: http://hdl.handle.net/2445/128207
ISSN: 1860-5397
Appears in Collections:Articles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica)

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