A convenient preparation of 9 H -carbazole-3,6-dicarbonitrile and 9 H -carbazole-3,6-dicarboxylic acid

Handle URI:
http://hdl.handle.net/10754/563350
Title:
A convenient preparation of 9 H -carbazole-3,6-dicarbonitrile and 9 H -carbazole-3,6-dicarboxylic acid
Authors:
Weselinski, Lukasz Jan ( 0000-0003-4516-2727 ) ; Luebke, Ryan ( 0000-0002-1285-3321 ) ; Eddaoudi, Mohamed ( 0000-0003-1916-9837 )
Abstract:
A catalytic, high yielding and scalable procedure for the synthesis of 9H-carbazole-3,6-dicarbonitrile has been developed. Subsequent hydrolysis of the dinitrile in the presence of a catalytic copper species (i.e., CuI) yields 9H-carbazole-3,6-dicarboxylic acid. Both compounds are versatile and fine-tunable organic building blocks and therefore offer potential in material science, medicinal and supramolecular chemistry. © Georg Thieme Verlag Stuttgart New York.
KAUST Department:
Advanced Membranes and Porous Materials Research Center; Physical Sciences and Engineering (PSE) Division; Chemical Science Program; Functional Materials Design, Discovery and Development (FMD3)
Publisher:
Thieme Publishing Group
Journal:
Synthesis
Issue Date:
23-Jan-2014
DOI:
10.1055/s-0033-1340557
Type:
Article
ISSN:
00397881
Sponsors:
The authors gratefully acknowledge KAUST for funding.
Is Supplemented By:
Weselinski, L., Luebke, R., & Eddaoudi, M. (2014). CCDC 938820: Experimental Crystal Structure Determination [Data set]. Cambridge Crystallographic Data Centre. https://doi.org/10.5517/cc10hxjy; DOI:10.5517/cc10hxjy; HANDLE:http://hdl.handle.net/10754/624217
Appears in Collections:
Articles; Advanced Membranes and Porous Materials Research Center; Physical Sciences and Engineering (PSE) Division; Functional Materials Design, Discovery and Development (FMD3); Chemical Science Program

Full metadata record

DC FieldValue Language
dc.contributor.authorWeselinski, Lukasz Janen
dc.contributor.authorLuebke, Ryanen
dc.contributor.authorEddaoudi, Mohameden
dc.date.accessioned2015-08-03T11:46:23Zen
dc.date.available2015-08-03T11:46:23Zen
dc.date.issued2014-01-23en
dc.identifier.issn00397881en
dc.identifier.doi10.1055/s-0033-1340557en
dc.identifier.urihttp://hdl.handle.net/10754/563350en
dc.description.abstractA catalytic, high yielding and scalable procedure for the synthesis of 9H-carbazole-3,6-dicarbonitrile has been developed. Subsequent hydrolysis of the dinitrile in the presence of a catalytic copper species (i.e., CuI) yields 9H-carbazole-3,6-dicarboxylic acid. Both compounds are versatile and fine-tunable organic building blocks and therefore offer potential in material science, medicinal and supramolecular chemistry. © Georg Thieme Verlag Stuttgart New York.en
dc.description.sponsorshipThe authors gratefully acknowledge KAUST for funding.en
dc.publisherThieme Publishing Groupen
dc.subjectcarbazolesen
dc.subjectcatalytic cyanationen
dc.subjectheterocyclesen
dc.subjectmetal-organic frameworksen
dc.subjectpalladium catalysisen
dc.subjectsupramolecular chemistryen
dc.titleA convenient preparation of 9 H -carbazole-3,6-dicarbonitrile and 9 H -carbazole-3,6-dicarboxylic aciden
dc.typeArticleen
dc.contributor.departmentAdvanced Membranes and Porous Materials Research Centeren
dc.contributor.departmentPhysical Sciences and Engineering (PSE) Divisionen
dc.contributor.departmentChemical Science Programen
dc.contributor.departmentFunctional Materials Design, Discovery and Development (FMD3)en
dc.identifier.journalSynthesisen
kaust.authorWeselinski, Lukasz Janen
kaust.authorLuebke, Ryanen
kaust.authorEddaoudi, Mohameden
dc.relation.isSupplementedByWeselinski, L., Luebke, R., & Eddaoudi, M. (2014). CCDC 938820: Experimental Crystal Structure Determination [Data set]. Cambridge Crystallographic Data Centre. https://doi.org/10.5517/cc10hxjyen
dc.relation.isSupplementedByDOI:10.5517/cc10hxjyen
dc.relation.isSupplementedByHANDLE:http://hdl.handle.net/10754/624217en
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