A rapid intramolecular imino Diels-Alder reaction of aminoanthraquinones with citronellal or prenylated salicylaldehydes: Substituent effect on changing the reaction pathway from Diels-Alder to ene-type cyclization

dc.contributor.author Gaddam, Vikram
dc.contributor.author Meesala, Ramu
dc.contributor.author Nagarajan, Rajagopal
dc.date.accessioned 2022-03-27T08:40:44Z
dc.date.available 2022-03-27T08:40:44Z
dc.date.issued 2007-08-16
dc.description.abstract The reaction of 1-aminoanthraquinone with citronellal or substituted prenylated salicylaldehyde catalyzed by triphenylphosphonium perchlorate (TPPP) is reported. The nature of the substituents in salicylaldehyde changes the reaction pathway from Diels-Alder to ene-type cyclization. © Georg Thieme Verlag Stuttgart.
dc.identifier.citation Synthesis
dc.identifier.issn 00397881
dc.identifier.uri 10.1055/s-2007-983790
dc.identifier.uri http://www.thieme-connect.de/DOI/DOI?10.1055/s-2007-983790
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/11468
dc.subject Aminoanthraquinones
dc.subject Chromanoquinolonaphthaquinones
dc.subject Cycloaddition
dc.subject Ene-type cyclization
dc.subject Naphthoacridine-5,14-dione
dc.title A rapid intramolecular imino Diels-Alder reaction of aminoanthraquinones with citronellal or prenylated salicylaldehydes: Substituent effect on changing the reaction pathway from Diels-Alder to ene-type cyclization
dc.type Journal. Article
dspace.entity.type
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