Unprecedented Alkene Transposition in Phthalate-Amino Acid Adducts

DC FieldValueLanguage
dc.contributor.authorSaha, Ishika-
dc.contributor.authorBaxendale, Ian R.-
dc.contributor.authorBaumann, Marcus-
dc.date.accessioned2021-11-09T16:14:27Z-
dc.date.available2021-11-09T16:14:27Z-
dc.date.copyright2018 Georg Thiemeen_US
dc.date.issued2018-11-07-
dc.identifier.citationSynletten_US
dc.identifier.issn0936-5214-
dc.identifier.urihttp://hdl.handle.net/10197/12607-
dc.description.abstractA detailed account on the outcome of the thermal reaction between benzylidene phthalides and various amino acid derivatives is reported. It was discovered that the tricyclic pyrroles as previously described are not the products formed in these reactions. Instead under high-temperature conditions decarboxylated phthalamide adducts are formed within 5-10 minutes. Additionally, an unprecedented alkene transposition mechanism has been identified leading to the final products of these reactions.en_US
dc.language.isoenen_US
dc.publisherGeorg Thiemeen_US
dc.subjectPhthalideen_US
dc.subjectPhthalamideen_US
dc.subjectTricyclic pyrroleen_US
dc.subjectAlkene transpositionen_US
dc.subjectPolycyclic Pyrroleen_US
dc.titleUnprecedented Alkene Transposition in Phthalate-Amino Acid Adductsen_US
dc.typeJournal Articleen_US
dc.internal.authorcontactothermarcus.baumann@ucd.ieen_US
dc.statusPeer revieweden_US
dc.identifier.volume29en_US
dc.identifier.issue20en_US
dc.identifier.startpage2648en_US
dc.identifier.endpage2654en_US
dc.identifier.doi10.1055/s-0037-1611294-
dc.neeo.contributorSaha|Ishika|aut|-
dc.neeo.contributorBaxendale|Ian R.|aut|-
dc.neeo.contributorBaumann|Marcus|aut|-
dc.description.othersponsorshipRoyal Societyen_US
dc.description.othersponsorshipSchool of Chemistry, University College Dublinen_US
dc.description.admin2020-10-06 JG: PDF replaced with correct versionen_US
dc.date.updated2020-09-21T18:36:20Z-
dc.rights.licensehttps://creativecommons.org/licenses/by-nc-nd/3.0/ie/en_US
item.fulltextWith Fulltext-
item.grantfulltextopen-
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