Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12779/6095
DC FieldValueLanguage
dc.contributor.authorAndrea, Porchedduen_us
dc.contributor.authorManuel G., Muraen_us
dc.contributor.authorLidia De, Lucaen_us
dc.contributor.authorPizzetti, Mariannaen_us
dc.contributor.authorTaddei, Maurizioen_us
dc.date.accessioned2021-03-30T15:59:38Z-
dc.date.available2021-03-30T15:59:38Z-
dc.date.issued2012-
dc.identifier.issn1523-7060en_US
dc.identifier.urihttp://hdl.handle.net/20.500.12779/6095-
dc.description57842en_US
dc.description.abstractIn a new version of the Fischer indole synthesis, primary and secondary alcohols have been catalytically oxidized in the presence of phenylhydrazines and protic or Lewis acids to give the corresponding indoles. The overall reaction can be accomplished in one step, and the use of alcohols instead of aldehyes or ketones as starting materials has several advantages in terms of a large selection of reagents, easy handling, and safety of the processen_US
dc.language.isoenen_US
dc.relationNoneen_US
dc.relation.ispartofORGANIC LETTERSen_US
dc.titleFrom Alcohols to Indoles: A Tandem Ru Catalyzed Hydrogen-Transfer Fischer Indole Synthesisen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/ol3030956en_US
dc.identifier.scopus2-s2.0-84870866154en_US
dc.identifier.isiWOS:000311926000076en_US
dc.relation.volume14en_US
dc.description.firstpage6112en_US
dc.description.lastpage6115en_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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