Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12779/4893
DC FieldValueLanguage
dc.contributor.authorG., Minettoen_us
dc.contributor.authorTaddei, Maurizioen_us
dc.date.accessioned2021-03-30T15:45:21Z-
dc.date.available2021-03-30T15:45:21Z-
dc.date.issued2004-
dc.identifier.issn1523-7060en_US
dc.identifier.urihttp://hdl.handle.net/20.500.12779/4893-
dc.description22397en_US
dc.description.abstractAn array of tetrasubstituted pyrroles (and trisubstituted furans) was obtained using a simple three-step procedure. Functional homologation of a -ketoester with an aldehyde followed by oxidation gave a series of differently substituted 1,4-dicarbonyl compounds that can be rapidly cyclized with the Paal−Knorr procedure carried out under microwave irradiation.en_US
dc.language.isoenen_US
dc.relationNoneen_US
dc.relation.ispartofORGANIC LETTERSen_US
dc.titleMicrowave assisted Paal-Knorr reaction. A rapid approach to polysubstituted furans and pyrrolesen_US
dc.typeArticleen_US
dc.relation.volume6en_US
dc.description.firstpage389en_US
dc.description.lastpage392en_US
dc.description.thirdmissionNot applicableen_US
item.cerifentitytypePublications-
item.grantfulltextnone-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeArticle-
item.fulltextNo Fulltext-
crisitem.author.orcid0000-0001-8660-7580-
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