Dergi makalesi Açık Erişim
Yilmaz, Mehmet; Inal, Asl i Ustalar
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<identifier identifierType="URL">https://aperta.ulakbim.gov.tr/record/260157</identifier>
<creators>
<creator>
<creatorName>Yilmaz, Mehmet</creatorName>
<givenName>Mehmet</givenName>
<familyName>Yilmaz</familyName>
<affiliation>Kocaeli Univ, Fac Arts & Sci, Dept Chem, TR-41380 Kocaeli, Turkey</affiliation>
</creator>
<creator>
<creatorName>Inal, Asl i Ustalar</creatorName>
<givenName>Asl i Ustalar</givenName>
<familyName>Inal</familyName>
<affiliation>Kocaeli Univ, Fac Arts & Sci, Dept Chem, TR-41380 Kocaeli, Turkey</affiliation>
</creator>
</creators>
<titles>
<title>Microwave Assisted Synthesis Of 2,3-Dihydro-4H-Benzo[4,5]Thiazolo [3,2-A]Furo[2,3-D] Pyrimidin-4-Ones By Radical Addition Of 2-Hydroxy-4H-Benzo[4,5]Thiazolo[3,2-A] Pyrimidin-4-Ones To Various Conjugated Alkenes And Dienes Mediated Mn(Oac)(3)</title>
</titles>
<publisher>Aperta</publisher>
<publicationYear>2022</publicationYear>
<dates>
<date dateType="Issued">2022-01-01</date>
</dates>
<resourceType resourceTypeGeneral="Text">Journal article</resourceType>
<alternateIdentifiers>
<alternateIdentifier alternateIdentifierType="url">https://aperta.ulakbim.gov.tr/record/260157</alternateIdentifier>
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<relatedIdentifiers>
<relatedIdentifier relatedIdentifierType="DOI" relationType="IsIdenticalTo">10.1016/j.tet.2022.132806</relatedIdentifier>
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<rightsList>
<rights rightsURI="http://www.opendefinition.org/licenses/cc-by">Creative Commons Attribution</rights>
<rights rightsURI="info:eu-repo/semantics/openAccess">Open Access</rights>
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<descriptions>
<description descriptionType="Abstract">Synthesis of chemically important, novel 2,3-dihydro-4H-benzo [4,5]thiazolo [3,2-a]furo [2,3-d]pyr-imidin-4-one derivatives was approached in this work. These heterocyclic compounds were synthesized in good to excellent yields from the reaction of Mn(OAc)3 mediated radical addition of 2-hydroxy-4H- benzo [4,5]thiazolo [3,2-a]pyrimidin-4-one (1a-1f) derivatives to various conjugated alkenes (2a-2e, 2h) and dienes (2f, 2g, 2i) under microwave irradiation in mild conditions. Also, a different compound skeleton, 2,3-dihydrobenzo [4,5]imidazo [1,2-a]furo [2,3-d]pyrimidin-4(10H)-one 3a (90%), was obtained from the reaction of 2-hydroxy-10-methylbenzo [4,5]imidazo [1,2-a]pyrimidin-4(10H)-one (1g) and 1,1diphenylethylene (2h) for the first time. While no product was obtained with conventional method in radical addition reactions, dihydrofuropyrimidines (3a-z, 3a) were synthesized in excellent yields using microwave irradiating method at 150 ?, 350 W for 60 s. All isolated compounds were characterized by spectroscopic techniques (FTIR, H-1 NMR, C-13 NMR and( 19)F NMR) and HRMS analysis.(c) 2022 Elsevier Ltd. All rights reserved.</description>
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