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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 |
| URI: | http://hdl.handle.net/2445/128207 |
| Related resource: | https://doi.org/10.3762/bjoc.14.237 |
| ISSN: | 1860-5397 |
| Appears in Collections: | Articles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica) |
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|---|---|---|---|---|
| 683225.pdf | 365.34 kB | Adobe PDF | View/Open |
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