Suzuki Cross-Coupling Reaction of Aryl Halides With Arylboronic Acids Catalysed by Pd(ii)-Nay Zeolite

dc.contributor.author Bulut, Hatice
dc.contributor.author Artok, Levent
dc.contributor.author Yılmaz, Selahattin
dc.coverage.doi 10.1016/S0040-4039(02)02523-6
dc.date.accessioned 2016-05-31T13:00:53Z
dc.date.available 2016-05-31T13:00:53Z
dc.date.issued 2003
dc.description.abstract Pd(II)-exchanged NaY zeolite showed high activity in the Suzuki cross-coupling reactions of aryl bromides and iodides without added ligands. The DMF:water ratio, and the type and amount of base were found to be critical for the efficiency of the reaction. The catalyst is reusable after regeneration. en_US
dc.description.sponsorship Research Funding Office of IZTECH with project No. FEN 2000 01 en_US
dc.identifier.citation Bulut, H., Artok, L., and Yılmaz, S. (2003). Suzuki cross-coupling reaction of aryl halides with arylboronic acids catalysed by Pd(II)-NaY zeolite. Tetrahedron Letters, 44(2), 289-291. doi:10.1016/S0040-4039(02)02523-6 en_US
dc.identifier.doi 10.1016/S0040-4039(02)02523-6 en_US
dc.identifier.doi 10.1016/S0040-4039(02)02523-6
dc.identifier.issn 0040-4039
dc.identifier.issn 1873-3581
dc.identifier.issn 0040-4039
dc.identifier.issn 0931-7597
dc.identifier.issn 1522-2667
dc.identifier.scopus 2-s2.0-0037421031
dc.identifier.uri http://doi.org/10.1016/S0040-4039(02)02523-6
dc.identifier.uri https://hdl.handle.net/11147/4694
dc.language.iso en en_US
dc.publisher Elsevier Ltd. en_US
dc.relation.ispartof Tetrahedron Letters en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Boronic acid derivative en_US
dc.subject Bromine derivative en_US
dc.subject Iodine derivative en_US
dc.subject Regeneration en_US
dc.subject Base en_US
dc.title Suzuki Cross-Coupling Reaction of Aryl Halides With Arylboronic Acids Catalysed by Pd(ii)-Nay Zeolite en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.institutional Artok, Levent
gdc.author.institutional Yılmaz, Selahattin
gdc.author.yokid 22592
gdc.bip.impulseclass C4
gdc.bip.influenceclass C4
gdc.bip.popularityclass C5
gdc.coar.access open access
gdc.coar.type text::journal::journal article
gdc.collaboration.industrial false
gdc.description.department İzmir Institute of Technology. Chemistry en_US
gdc.description.department İzmir Institute of Technology. Chemical Engineering en_US
gdc.description.endpage 291 en_US
gdc.description.issue 2 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q3
gdc.description.startpage 289 en_US
gdc.description.volume 44 en_US
gdc.description.wosquality Q3
gdc.identifier.openalex W2177822848
gdc.identifier.wos WOS:000180321000019
gdc.index.type WoS
gdc.index.type Scopus
gdc.oaire.accesstype BRONZE
gdc.oaire.diamondjournal false
gdc.oaire.impulse 12.0
gdc.oaire.influence 5.3017604E-9
gdc.oaire.isgreen true
gdc.oaire.keywords Boronic acid derivative
gdc.oaire.keywords Regeneration
gdc.oaire.keywords Bromine derivative
gdc.oaire.keywords Base
gdc.oaire.keywords Iodine derivative
gdc.oaire.popularity 3.0737222E-9
gdc.oaire.publicfunded false
gdc.oaire.sciencefields 01 natural sciences
gdc.oaire.sciencefields 0104 chemical sciences
gdc.openalex.collaboration National
gdc.openalex.fwci 3.53588371
gdc.openalex.normalizedpercentile 0.93
gdc.openalex.toppercent TOP 10%
gdc.opencitations.count 49
gdc.plumx.crossrefcites 41
gdc.plumx.mendeley 19
gdc.plumx.scopuscites 59
gdc.scopus.citedcount 59
gdc.wos.citedcount 56
relation.isAuthorOfPublication.latestForDiscovery 383d88ac-56b2-4451-a813-f8456d2fa034
relation.isOrgUnitOfPublication.latestForDiscovery 9af2b05f-28ac-4021-8abe-a4dfe192da5e

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