Yayın:
Crystal structure of 1-{4-hydroxy-3-[(pyrrolidin-1-yl)methyl]phenyl}-3-phenylprop-2-en-1-one

Basit Görünüm
dc.contributor.authorYerdelen, Kadir Özden
dc.contributor.authorGül, Halise İnci
dc.contributor.authorAydin, Abdullah
dc.contributor.authorCelik, Raziye Catak
dc.contributor.authorAkkurt, Mehmet
dc.date.accessioned2026-01-02T23:38:22Z
dc.date.issued2016-04-15
dc.description.abstractIn the title compound, C20H21NO2, the pyrrolidine ring adopts an envelope conformation with the N atom at the flap position. The central benzene ring makes dihedral angles of 21.39 (10) and 80.10 (15)° with the phenyl ring and the mean plane of the pyrrolidine ring, respectively. The molecular conformation is stabilized by an intramolecular O—H...N hydrogen bond, which closes anS(6) ring. A weak C—H...π interaction is observed in the crystal.
dc.description.urihttps://doi.org/10.1107/s2056989016006009
dc.description.urihttp://journals.iucr.org/e/issues/2016/05/00/hb7576/hb7576.pdf
dc.description.urihttps://pubmed.ncbi.nlm.nih.gov/27308021
dc.description.urihttp://dx.doi.org/10.1107/S2056989016006009
dc.description.urihttps://doaj.org/article/584d605d3dd244bd9b8ac4802a524eb0
dc.description.urihttps://dx.doi.org/10.1107/s2056989016006009
dc.description.urihttps://doi.org/10.1107/S2056989016006009
dc.description.urihttps://hdl.handle.net/20.500.12451/4877
dc.description.urihttps://avesis.erciyes.edu.tr/publication/details/fc0b9e77-80da-4883-9d74-b90cdca171f9/oai
dc.description.urihttps://avesis.atauni.edu.tr/publication/details/fc0b9e77-80da-4883-9d74-b90cdca171f9/oai
dc.identifier.doi10.1107/s2056989016006009
dc.identifier.eissn2056-9890
dc.identifier.endpage698
dc.identifier.openairedoi_dedup___::b55e54deef864de0e76a5e23a348b1a3
dc.identifier.orcid0000-0001-6164-9602
dc.identifier.orcid0000-0003-2805-9314
dc.identifier.orcid0000-0003-2421-0929
dc.identifier.pubmed27308021
dc.identifier.scopus2-s2.0-84969535041
dc.identifier.startpage696
dc.identifier.urihttps://hdl.handle.net/20.500.12597/36161
dc.identifier.volume72
dc.identifier.wos000375489100023
dc.publisherInternational Union of Crystallography (IUCr)
dc.relation.ispartofActa Crystallographica Section E Crystallographic Communications
dc.rightsOPEN
dc.subjectcrystal structure
dc.subjectCrystallography
dc.subjectintramolecular O—H...N hydrogen bond
dc.subjectmethylphenyl
dc.subjectResearch Communications
dc.subjectMannich Bases
dc.subjectintramolecular O-H center dot center dot center dot N hydrogen bond
dc.subjectQD901-999
dc.subjectMannich bases
dc.subjectSemi-Empirical
dc.subjectCrystal Structure
dc.subjectMethylphenyl
dc.subjectsemi-empirical
dc.subject.sdg3. Good health
dc.titleCrystal structure of 1-{4-hydroxy-3-[(pyrrolidin-1-yl)methyl]phenyl}-3-phenylprop-2-en-1-one
dc.typeArticle
dspace.entity.typePublication
local.api.response{"authors":[{"fullName":"YERDELEN, Kadir Özden","name":"Kadir Özden","surname":"Yerdelen","rank":1,"pid":null},{"fullName":"GÜL, Halise İnci","name":"Halise İnci","surname":"Gül","rank":2,"pid":{"id":{"scheme":"orcid","value":"0000-0001-6164-9602"},"provenance":null}},{"fullName":"AYDIN, ABDULLAH","name":"Abdullah","surname":"Aydin","rank":3,"pid":{"id":{"scheme":"orcid","value":"0000-0003-2805-9314"},"provenance":null}},{"fullName":"Celik, Raziye Catak","name":"Raziye Catak","surname":"Celik","rank":4,"pid":null},{"fullName":"AKKURT, MEHMET","name":"Mehmet","surname":"Akkurt","rank":5,"pid":{"id":{"scheme":"orcid","value":"0000-0003-2421-0929"},"provenance":null}}],"openAccessColor":"gold","publiclyFunded":false,"type":"publication","language":{"code":"und","label":"Undetermined"},"countries":null,"subjects":[{"subject":{"scheme":"FOS","value":"0301 basic medicine"},"provenance":null},{"subject":{"scheme":"keyword","value":"crystal structure"},"provenance":null},{"subject":{"scheme":"FOS","value":"0303 health sciences"},"provenance":null},{"subject":{"scheme":"keyword","value":"Crystallography"},"provenance":null},{"subject":{"scheme":"keyword","value":"intramolecular O—H...N hydrogen bond"},"provenance":null},{"subject":{"scheme":"keyword","value":"methylphenyl"},"provenance":null},{"subject":{"scheme":"keyword","value":"Research Communications"},"provenance":null},{"subject":{"scheme":"SDG","value":"3. Good health"},"provenance":null},{"subject":{"scheme":"keyword","value":"Mannich Bases"},"provenance":null},{"subject":{"scheme":"keyword","value":"intramolecular O-H center dot center dot center dot N hydrogen bond"},"provenance":null},{"subject":{"scheme":"FOS","value":"03 medical and health sciences"},"provenance":null},{"subject":{"scheme":"keyword","value":"QD901-999"},"provenance":null},{"subject":{"scheme":"keyword","value":"Mannich bases"},"provenance":null},{"subject":{"scheme":"keyword","value":"Semi-Empirical"},"provenance":null},{"subject":{"scheme":"keyword","value":"Crystal Structure"},"provenance":null},{"subject":{"scheme":"keyword","value":"Methylphenyl"},"provenance":null},{"subject":{"scheme":"keyword","value":"semi-empirical"},"provenance":null}],"mainTitle":"Crystal structure of 1-{4-hydroxy-3-[(pyrrolidin-1-yl)methyl]phenyl}-3-phenylprop-2-en-1-one","subTitle":null,"descriptions":["<jats:p>In the title compound, C<jats:sub>20</jats:sub>H<jats:sub>21</jats:sub>NO<jats:sub>2</jats:sub>, the pyrrolidine ring adopts an envelope conformation with the N atom at the flap position. The central benzene ring makes dihedral angles of 21.39 (10) and 80.10 (15)° with the phenyl ring and the mean plane of the pyrrolidine ring, respectively. The molecular conformation is stabilized by an intramolecular O—H...N hydrogen bond, which closes an<jats:italic>S</jats:italic>(6) ring. A weak C—H...π interaction is observed in the crystal.</jats:p>"],"publicationDate":"2016-04-15","publisher":"International Union of Crystallography (IUCr)","embargoEndDate":null,"sources":["Crossref","Acta Crystallogr E Crystallogr Commun","Acta Crystallographica Section E: Crystallographic Communications, Vol 72, Iss 5, Pp 696-698 (2016)"],"formats":["application/pdf"],"contributors":null,"coverages":null,"bestAccessRight":{"code":"c_abf2","label":"OPEN","scheme":"http://vocabularies.coar-repositories.org/documentation/access_rights/"},"container":{"name":"Acta Crystallographica Section E Crystallographic Communications","issnPrinted":null,"issnOnline":"2056-9890","issnLinking":null,"ep":"698","iss":null,"sp":"696","vol":"72","edition":null,"conferencePlace":null,"conferenceDate":null},"documentationUrls":null,"codeRepositoryUrl":null,"programmingLanguage":null,"contactPeople":null,"contactGroups":null,"tools":null,"size":null,"version":null,"geoLocations":null,"id":"doi_dedup___::b55e54deef864de0e76a5e23a348b1a3","originalIds":["S2056989016006009","10.1107/s2056989016006009","50|doiboost____|b55e54deef864de0e76a5e23a348b1a3","od_______267::369781b19d32ba98e9d3495728048e85","27308021","PMC4908517","oai:pubmedcentral.nih.gov:4908517","50|od_______267::369781b19d32ba98e9d3495728048e85","oai:doaj.org/article:584d605d3dd244bd9b8ac4802a524eb0","50|doajarticles::2fb391907b1f7e76f507abda2b96e90b","2340046937","50|od______4866::57deac76b5d7ce81496cad7c8c83f185","oai:acikerisim.aksaray.edu.tr:20.500.12451/4877","fc0b9e77-80da-4883-9d74-b90cdca171f9","50|od______9447::6538576e323700bcf02dd9ed8bfc11e7","50|od______9933::6538576e323700bcf02dd9ed8bfc11e7"],"pids":[{"scheme":"doi","value":"10.1107/s2056989016006009"},{"scheme":"pmid","value":"27308021"},{"scheme":"pmc","value":"PMC4908517"},{"scheme":"handle","value":"20.500.12451/4877"}],"dateOfCollection":null,"lastUpdateTimeStamp":null,"indicators":{"citationImpact":{"citationCount":0,"influence":2.5349236e-9,"popularity":8.410903e-10,"impulse":0,"citationClass":"C5","influenceClass":"C5","impulseClass":"C5","popularityClass":"C5"}},"instances":[{"pids":[{"scheme":"doi","value":"10.1107/s2056989016006009"}],"license":"CC BY","type":"Article","urls":["https://doi.org/10.1107/s2056989016006009"],"publicationDate":"2016-04-15","refereed":"peerReviewed"},{"pids":[{"scheme":"doi","value":"10.1107/s2056989016006009"}],"license":"CC BY","type":"Article","urls":["http://journals.iucr.org/e/issues/2016/05/00/hb7576/hb7576.pdf"],"refereed":"nonPeerReviewed"},{"pids":[{"scheme":"pmid","value":"27308021"},{"scheme":"pmc","value":"PMC4908517"}],"alternateIdentifiers":[{"scheme":"doi","value":"10.1107/s2056989016006009"}],"type":"Article","urls":["https://pubmed.ncbi.nlm.nih.gov/27308021"],"publicationDate":"2016-06-16","refereed":"nonPeerReviewed"},{"alternateIdentifiers":[{"scheme":"doi","value":"10.1107/s2056989016006009"}],"license":"CC BY","type":"Other literature type","urls":["http://dx.doi.org/10.1107/S2056989016006009"],"publicationDate":"2016-04-15","refereed":"nonPeerReviewed"},{"alternateIdentifiers":[{"scheme":"doi","value":"10.1107/s2056989016006009"}],"type":"Article","urls":["https://doaj.org/article/584d605d3dd244bd9b8ac4802a524eb0"],"publicationDate":"2016-05-01","refereed":"nonPeerReviewed"},{"alternateIdentifiers":[{"scheme":"doi","value":"10.1107/s2056989016006009"},{"scheme":"mag_id","value":"2340046937"}],"type":"Article","urls":["https://dx.doi.org/10.1107/s2056989016006009"],"refereed":"nonPeerReviewed"},{"pids":[{"scheme":"handle","value":"20.500.12451/4877"}],"alternateIdentifiers":[{"scheme":"doi","value":"10.1107/s2056989016006009"}],"type":"Article","urls":["https://doi.org/10.1107/S2056989016006009","https://hdl.handle.net/20.500.12451/4877"],"publicationDate":"2019-07-13","refereed":"nonPeerReviewed"},{"alternateIdentifiers":[{"scheme":"doi","value":"10.1107/s2056989016006009"}],"type":"Article","urls":["https://avesis.erciyes.edu.tr/publication/details/fc0b9e77-80da-4883-9d74-b90cdca171f9/oai"],"publicationDate":"2016-05-01","refereed":"nonPeerReviewed"},{"alternateIdentifiers":[{"scheme":"doi","value":"10.1107/s2056989016006009"}],"type":"Article","urls":["https://avesis.atauni.edu.tr/publication/details/fc0b9e77-80da-4883-9d74-b90cdca171f9/oai"],"publicationDate":"2016-05-01","refereed":"nonPeerReviewed"}],"isGreen":true,"isInDiamondJournal":false}
local.import.sourceOpenAire
local.indexed.atWOS
local.indexed.atScopus
local.indexed.atPubMed

Dosyalar

Koleksiyonlar

Publications