dc.contributor.author
Saborit Villarroya, Gisela
dc.contributor.author
Cativiela, Carlos
dc.contributor.author
Jimenez, Ana I.
dc.contributor.author
Bonjoch i Sesé, Josep
dc.contributor.author
Bradshaw, Ben
dc.date.issued
2019-02-13T12:54:14Z
dc.date.issued
2019-02-13T12:54:14Z
dc.date.issued
2018-10-09
dc.date.issued
2019-02-13T12:54:14Z
dc.identifier
https://hdl.handle.net/2445/128207
dc.description.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
dc.format
application/pdf
dc.publisher
Beilstein Institute
dc.relation
Reproducció del document publicat a: https://doi.org/10.3762/bjoc.14.237
dc.relation
Beilstein Journal of Organic Chemistry, 2018, vol. 14, p. 2597-2601
dc.relation
https://doi.org/10.3762/bjoc.14.237
dc.rights
cc-by (c) Saborit Villarroya, Gisela et al., 2018
dc.rights
http://creativecommons.org/licenses/by/3.0/es
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Articles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica)
dc.subject
Ciclització (Química)
dc.subject
Síntesi orgànica
dc.subject
Ring formation (Chemistry)
dc.subject
Organic synthesis
dc.title
Synthesis of cis-hydrindan-2,4-diones bearing an all.carbon quaternary center by a Danheiser annulation
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion
