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dc.contributor.authorDiana-Rivero, Raquel
dc.contributor.authorHalsvik, Beate
dc.contributor.authorGarciá Tellado, Fernando
dc.contributor.authorTejedor, David
dc.date.accessioned2022-04-04T10:44:41Z
dc.date.available2022-04-04T10:44:41Z
dc.date.created2022-01-25T09:34:38Z
dc.date.issued2021
dc.identifier.issn1523-7060
dc.identifier.urihttps://hdl.handle.net/11250/2989533
dc.description.abstractWe herein describe a simple and metal-free domino methodology to synthesize 2-aminopyrroles from alkynyl vinyl hydrazides. The domino reaction involves a novel propargylic 3,4-diaza-Cope rearrangement and a tandem isomerization/5-exo-dig N-cyclization reaction. By using this approach, a number of 2-aminopyrroles with diverse substituents have been prepared.en_US
dc.language.isoengen_US
dc.publisherAmerican Chemical Societyen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleShort and Modular Synthesis of Substituted 2‑Aminopyrrolesen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2021 American Chemical Societyen_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2
dc.identifier.doi10.1021/acs.orglett.1c01345
dc.identifier.cristin1989133
dc.source.journalOrganic Lettersen_US
dc.source.pagenumber4078-4082en_US
dc.identifier.citationOrganic Letters. 2021, 23 (10), 4078-4082.en_US
dc.source.volume23en_US
dc.source.issue10en_US


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Navngivelse 4.0 Internasjonal
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