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dc.contributor.authorAnga, Srinivas-
dc.contributor.authorChandra, Shubhadeep-
dc.contributor.authorSarkar, Pallavi-
dc.contributor.authorDas, Shubhajit-
dc.contributor.authorMandal, Debdeep-
dc.contributor.authorKundu, Abhinanda-
dc.contributor.authorRawat, Hemant-
dc.contributor.authorSchulzke, Carola-
dc.contributor.authorSarkar, Biprajit-
dc.contributor.authorPati, Swapan K.-
dc.contributor.authorChandrasekhar, Vadapalli-
dc.contributor.authorJana, Anukul-
dc.date.accessioned2024-05-27T12:39:02Z-
dc.date.available2024-05-27T12:39:02Z-
dc.date.issued2020de
dc.identifier.issn1099-0690-
dc.identifier.issn1434-193X-
dc.identifier.other1890811823-
dc.identifier.urihttp://nbn-resolving.de/urn:nbn:de:bsz:93-opus-ds-144252de
dc.identifier.urihttp://elib.uni-stuttgart.de/handle/11682/14425-
dc.identifier.urihttp://dx.doi.org/10.18419/opus-14406-
dc.description.abstractHerein, we report the synthesis of a series of push–pull imines by considering cyclic diamino substituent at the C‐centre and fluoroaryl substituent at the N‐centre. This has been achieved by a selective aromatic nucleophilic substitution of different fluoroarenes by N‐H‐substituted N‐heterocyclic imines (NHIs) at ambient conditions without any additional reagent. Solid‐state molecular structure analysis reveals the elongation of the central C-N bond of the imine functionality, which is consistent with the push–pull nature of these imines. The push-pull nature of these imines is further validated by computational studies.en
dc.description.sponsorshipTIFR Hyderabadde
dc.description.sponsorshipDeutsche Forschungsgemeinschaftde
dc.language.isoende
dc.relation.uridoi:10.1002/ejoc.202001344de
dc.rightsinfo:eu-repo/semantics/openAccessde
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/de
dc.subject.ddc540de
dc.titleFacile one‐pot assembly of push-pull imines by a selective C-F substitution process in aryl fluoridesen
dc.typearticlede
dc.date.updated2023-11-14T05:07:34Z-
ubs.fakultaetChemiede
ubs.fakultaetFakultätsübergreifend / Sonstige Einrichtungde
ubs.institutInstitut für Anorganische Chemiede
ubs.institutFakultätsübergreifend / Sonstige Einrichtungde
ubs.publikation.seiten7445-7449de
ubs.publikation.sourceEuropean journal of organic chemistry 2020 (2020), S. 7445-7449de
ubs.publikation.typZeitschriftenartikelde
Enthalten in den Sammlungen:03 Fakultät Chemie

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