Synthesis of Stilbene-Fused 2'-hydroxychalcones and Flavanones

dc.contributor.author Akçok, İsmail
dc.contributor.author Çağır, Ali
dc.coverage.doi 10.1016/j.bioorg.2010.04.001
dc.date.accessioned 2016-12-27T12:35:16Z
dc.date.available 2016-12-27T12:35:16Z
dc.date.issued 2010
dc.description.abstract Synthesis of stilbene-fused chalcones and flavanones were successfully completed. Molecules were designed in a way to mimic the structural features of both "stilbene and chalcones" or "stilbene and flavanones" at the same time, and synthesized by three steps. Heck reactions of 3-bromobenzaldehyde with styrene derivatives gave corresponding (E)-stilbenes, which were reacted with acetophenones to furnish stilbene-fused 2′-hydroxychalcones under basic conditions. Finally, intramolecular cyclization reactions were performed to produce stilbene-fused flavanones. © 2010 Elsevier Inc. en_US
dc.description.sponsorship DPT Research Grant DPT-2003K120690 (DPT10) en_US
dc.identifier.citation Akçok, İ., and Çağır, A. (2010). Synthesis of stilbene-fused 2′-hydroxychalcones and flavanones. Bioorganic Chemistry, 38(4), 139-143. doi:10.1016/j.bioorg.2010.04.001 en_US
dc.identifier.doi 10.1016/j.bioorg.2010.04.001
dc.identifier.doi 10.1016/j.bioorg.2010.04.001 en_US
dc.identifier.issn 0045-2068
dc.identifier.scopus 2-s2.0-77954212534
dc.identifier.uri http://doi.org/10.1016/j.bioorg.2010.04.001
dc.identifier.uri https://hdl.handle.net/11147/2685
dc.language.iso en en_US
dc.publisher Elsevier Ltd. en_US
dc.relation.ispartof Bioorganic Chemistry en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Chalcone en_US
dc.subject Flavanone en_US
dc.subject Heck reaction en_US
dc.subject Michael addition en_US
dc.subject Stilbene en_US
dc.title Synthesis of Stilbene-Fused 2'-hydroxychalcones and Flavanones en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.institutional Akçok, İsmail
gdc.author.institutional Çağır, Ali
gdc.author.yokid 110975
gdc.bip.impulseclass C4
gdc.bip.influenceclass C5
gdc.bip.popularityclass C4
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.endpage 143 en_US
gdc.description.issue 4 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q1
gdc.description.startpage 139 en_US
gdc.description.volume 38 en_US
gdc.description.wosquality Q1
gdc.identifier.openalex W2001098118
gdc.identifier.pmid 20457464
gdc.identifier.wos WOS:000285403000001
gdc.index.type WoS
gdc.index.type Scopus
gdc.index.type PubMed
gdc.oaire.accesstype BRONZE
gdc.oaire.diamondjournal false
gdc.oaire.impulse 5.0
gdc.oaire.influence 3.5515166E-9
gdc.oaire.isgreen true
gdc.oaire.keywords Heck reaction
gdc.oaire.keywords Chalcone
gdc.oaire.keywords Chalcones
gdc.oaire.keywords Cyclization
gdc.oaire.keywords Michael addition
gdc.oaire.keywords Stilbene
gdc.oaire.keywords Flavanones
gdc.oaire.keywords Stilbenes
gdc.oaire.keywords Flavanone
gdc.oaire.popularity 9.07188E-9
gdc.oaire.publicfunded false
gdc.oaire.sciencefields 01 natural sciences
gdc.oaire.sciencefields 0104 chemical sciences
gdc.openalex.collaboration National
gdc.openalex.fwci 1.76947847
gdc.openalex.normalizedpercentile 0.82
gdc.opencitations.count 17
gdc.plumx.crossrefcites 16
gdc.plumx.mendeley 27
gdc.plumx.pubmedcites 5
gdc.plumx.scopuscites 19
gdc.scopus.citedcount 19
gdc.wos.citedcount 19
relation.isAuthorOfPublication.latestForDiscovery 95611ee0-9a5b-4ec8-90ea-22896ec18aa9
relation.isOrgUnitOfPublication.latestForDiscovery 9af2b05f-28ac-4011-8abe-a4dfe192da5e

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