Reactions of Acyl Phosphonates With Organoaluminum Reagents: a New Method for the Synthesis of Secondary and Tertiary ?-Hydroxy Phosphonates

dc.contributor.author Seven, Özlem
dc.contributor.author Polat Çakır, Sıdıka
dc.contributor.author Hossain, Mohammad Shakhawoat
dc.contributor.author Emrullahoğlu, Mustafa
dc.contributor.author Demir, Ayhan Sıtkı
dc.coverage.doi 10.1016/j.tet.2011.03.036
dc.date.accessioned 2017-03-16T06:58:12Z
dc.date.available 2017-03-16T06:58:12Z
dc.date.issued 2011
dc.description.abstract The reactions of organoaluminum reagents (trimethylaluminum, triethylaluminum, etc.) with aryl and alkyl acyl phosphonates, which lead to the formation of α-hydroxy phosphonates in moderate to good yields, are reported. This method provides easy access to secondary and tertiary α-hydroxy phosphonates depending on the reaction conditions. The reactions of triethyl en_US
dc.description.sponsorship Scientific and Technological Research Council of Turkey; Turkish Academy of Science; Middle East Technical University en_US
dc.identifier.citation Seven, O., Polat Çakır, S., Hossain, M.S., Emrullahoğlu, M., and Demir, A. S. (2011). Reactions of acyl phosphonates with organoaluminum reagents: A new method for the synthesis of secondary and tertiary α-hydroxy phosphonates. Tetrahedron, 67(19), 3464-3469. doi:10.1016/j.tet.2011.03.036 en_US
dc.identifier.doi 10.1016/j.tet.2011.03.036
dc.identifier.doi 10.1016/j.tet.2011.03.036 en_US
dc.identifier.issn 0040-4020
dc.identifier.issn 1464-5416
dc.identifier.issn 0931-7597
dc.identifier.issn 1522-2667
dc.identifier.scopus 2-s2.0-79955028627
dc.identifier.uri https://doi.org/10.1016/j.tet.2011.03.036
dc.identifier.uri https://hdl.handle.net/11147/5070
dc.language.iso en en_US
dc.publisher Elsevier Ltd. en_US
dc.relation.ispartof Tetrahedron en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject α-Hydroxy phosphonates en_US
dc.subject Acyl phosphonates en_US
dc.subject Organoaluminum en_US
dc.subject Organometallic compound en_US
dc.title Reactions of Acyl Phosphonates With Organoaluminum Reagents: a New Method for the Synthesis of Secondary and Tertiary ?-Hydroxy Phosphonates en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.institutional Emrullahoğlu, Mustafa
gdc.author.yokid 203331
gdc.bip.impulseclass C5
gdc.bip.influenceclass C5
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.endpage 3469 en_US
gdc.description.issue 19 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q3
gdc.description.startpage 3464 en_US
gdc.description.volume 67 en_US
gdc.description.wosquality Q2
gdc.identifier.openalex W2950023740
gdc.identifier.wos WOS:000290602000023
gdc.index.type WoS
gdc.index.type Scopus
gdc.oaire.accesstype BRONZE
gdc.oaire.diamondjournal false
gdc.oaire.impulse 4.0
gdc.oaire.influence 3.1881038E-9
gdc.oaire.isgreen true
gdc.oaire.keywords Organoaluminum
gdc.oaire.keywords α-Hydroxy phosphonates
gdc.oaire.keywords Organometallic compound
gdc.oaire.keywords Acyl phosphonates
gdc.oaire.popularity 2.7132283E-9
gdc.oaire.publicfunded false
gdc.oaire.sciencefields 01 natural sciences
gdc.oaire.sciencefields 0104 chemical sciences
gdc.openalex.collaboration National
gdc.openalex.fwci 1.0937199
gdc.openalex.normalizedpercentile 0.76
gdc.opencitations.count 16
gdc.plumx.crossrefcites 17
gdc.plumx.mendeley 9
gdc.plumx.scopuscites 19
gdc.scopus.citedcount 19
gdc.wos.citedcount 17
relation.isAuthorOfPublication.latestForDiscovery a0a3756c-8977-4835-98e6-00d06add57fb
relation.isOrgUnitOfPublication.latestForDiscovery 9af2b05f-28ac-4010-8abe-a4dfe192da5e

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