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dc.contributor.authorSaid, Awad I.
dc.contributor.authorPalkó, Márta
dc.contributor.authorHaukka, Matti
dc.contributor.authorFülöp, Ferenc
dc.date.accessioned2020-12-23T08:30:38Z
dc.date.available2020-12-23T08:30:38Z
dc.date.issued2020
dc.identifier.citationSaid, A. I., Palkó, M., Haukka, M., & Fülöp, F. (2020). Angular Regioselectivity in the Reactions of 2-Thioxopyrimidin-4-ones and Hydrazonoyl Chlorides : Synthesis of Novel Stereoisomeric Octahydro[1,2,4]triazolo[4,3-a]quinazolin-5-ones. <i>Molecules</i>, <i>25</i>(23), Article 5673. <a href="https://doi.org/10.3390/molecules25235673" target="_blank">https://doi.org/10.3390/molecules25235673</a>
dc.identifier.otherCONVID_47466044
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/73402
dc.description.abstractThe regioselective synthesis of cis and trans stereoisomers of variously functionalized octahydro[1,2,4]triazolo[4,3-a]quinazolin-5-ones was performed. The 2-thioxopyrimidin-4-ones used in the synthesis reacted with hydrazonoyl chlorides in a regioselective manner to produce the angular regioisomers [1,2,4]triazolo[4,3-a]quinazolin-5-ones rather than the linear isomers [1,2,4]triazolo[4,3-a]quinazolin-5-ones. The synthesis process took place with electronic control. The angular regiochemistry of the products was confirmed by X-ray experiments and two-dimensional NMR studies.en
dc.format.mimetypeapplication/pdf
dc.languageeng
dc.language.isoeng
dc.publisherMDPI
dc.relation.ispartofseriesMolecules
dc.rightsCC BY 4.0
dc.subject.otherregioselective reactions
dc.subject.otherhydrazonoyl chlorides
dc.subject.other2-thioxopyrimidin-4-ones
dc.subject.other[1,2,4]triazolo[4,3-a]quinazolin-5-ones
dc.titleAngular Regioselectivity in the Reactions of 2-Thioxopyrimidin-4-ones and Hydrazonoyl Chlorides : Synthesis of Novel Stereoisomeric Octahydro[1,2,4]triazolo[4,3-a]quinazolin-5-ones
dc.typeresearch article
dc.identifier.urnURN:NBN:fi:jyu-202012237343
dc.contributor.laitosKemian laitosfi
dc.contributor.laitosDepartment of Chemistryen
dc.contributor.oppiaineEpäorgaaninen kemiafi
dc.contributor.oppiaineEpäorgaaninen ja analyyttinen kemiafi
dc.contributor.oppiaineInorganic Chemistryen
dc.contributor.oppiaineInorganic and Analytical Chemistryen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.relation.issn1420-3049
dc.relation.numberinseries23
dc.relation.volume25
dc.type.versionpublishedVersion
dc.rights.copyright© 2020 the Authors
dc.rights.accesslevelopenAccessfi
dc.type.publicationarticle
dc.subject.ysoorgaaniset yhdisteet
dc.subject.ysokemiallinen synteesi
dc.subject.ysoisomeria
dc.subject.ysotyppiyhdisteet
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p3841
jyx.subject.urihttp://www.yso.fi/onto/yso/p8468
jyx.subject.urihttp://www.yso.fi/onto/yso/p10129
jyx.subject.urihttp://www.yso.fi/onto/yso/p640
dc.rights.urlhttps://creativecommons.org/licenses/by/4.0/
dc.relation.doi10.3390/molecules25235673
jyx.fundinginformationWe are grateful to the Hungarian Research Foundation (OTKA No. K 115731). The financial support of the GINOP-2.3.2-15-2016-00014 project is acknowledged. The Ministry of Human Capacities, Hungary, grant TUDFO/47138-1/2019, is acknowledged.
dc.type.okmA1


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