Synthesis of cis-hydrindan-2, 4-diones bearing an all-carbon quaternary center by a Danheiser annulation
Resumen: 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 beta-keto ester.
Idioma: Inglés
DOI: 10.3762/bjoc.14.237
Año: 2018
Publicado en: BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY 14 (2018), 2597-2601
ISSN: 1860-5397

Factor impacto JCR: 2.595 (2018)
Categ. JCR: CHEMISTRY, ORGANIC rank: 20 / 57 = 0.351 (2018) - Q2 - T2
Factor impacto SCIMAGO: 0.821 - Organic Chemistry (Q2)

Financiación: info:eu-repo/grantAgreement/ES/DGA/E19-17R
Financiación: info:eu-repo/grantAgreement/ES/MINECO/CTQ2013-40855-R
Financiación: info:eu-repo/grantAgreement/ES/MINECO/CTQ2016-41338-P
Tipo y forma: Article (Published version)
Área (Departamento): Área Química Orgánica (Dpto. Química Orgánica)

Creative Commons You must give appropriate credit, provide a link to the license, and indicate if changes were made. You may do so in any reasonable manner, but not in any way that suggests the licensor endorses you or your use.


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 Record created 2018-11-28, last modified 2019-11-22


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