Dergi makalesi Açık Erişim
Altug, Cevher; Buyukbayram, Muhammet; Kavas, Ozge; Yavuz, Muhsine Zeynep
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<identifier identifierType="URL">https://aperta.ulakbim.gov.tr/record/63689</identifier>
<creators>
<creator>
<creatorName>Altug, Cevher</creatorName>
<givenName>Cevher</givenName>
<familyName>Altug</familyName>
<affiliation>Abant Izzet Baysal Univ, Dept Chem, TR-14280 Bolu, Turkey</affiliation>
</creator>
<creator>
<creatorName>Buyukbayram, Muhammet</creatorName>
<givenName>Muhammet</givenName>
<familyName>Buyukbayram</familyName>
<affiliation>Abant Izzet Baysal Univ, Dept Chem, TR-14280 Bolu, Turkey</affiliation>
</creator>
<creator>
<creatorName>Kavas, Ozge</creatorName>
<givenName>Ozge</givenName>
<familyName>Kavas</familyName>
<affiliation>Abant Izzet Baysal Univ, Dept Chem, TR-14280 Bolu, Turkey</affiliation>
</creator>
<creator>
<creatorName>Yavuz, Muhsine Zeynep</creatorName>
<givenName>Muhsine Zeynep</givenName>
<familyName>Yavuz</familyName>
<affiliation>Abant Izzet Baysal Univ, Fac Med, Dept Med Pharmacol, TR-14280 Bolu, Turkey</affiliation>
</creator>
</creators>
<titles>
<title>A Green Synthesis Of New 3-Aryl-4-Phenylsulfonyl-5-Aminoisoxazoles</title>
</titles>
<publisher>Aperta</publisher>
<publicationYear>2014</publicationYear>
<dates>
<date dateType="Issued">2014-01-01</date>
</dates>
<resourceType resourceTypeGeneral="Text">Journal article</resourceType>
<alternateIdentifiers>
<alternateIdentifier alternateIdentifierType="url">https://aperta.ulakbim.gov.tr/record/63689</alternateIdentifier>
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<relatedIdentifiers>
<relatedIdentifier relatedIdentifierType="DOI" relationType="IsIdenticalTo">10.1016/j.tet.2014.03.106</relatedIdentifier>
</relatedIdentifiers>
<rightsList>
<rights rightsURI="http://www.opendefinition.org/licenses/cc-by">Creative Commons Attribution</rights>
<rights rightsURI="info:eu-repo/semantics/openAccess">Open Access</rights>
</rightsList>
<descriptions>
<description descriptionType="Abstract">The present work describes a new protocol for the synthesis of 5-aminoisoxazoles using alpha-chlorooximes and 2-phenylsulfonyl acetonitrile via green chemistry routes. The titled 5-aminoisoxazoles 3 were further reacted with 4-nitrobenzoyl chloride to obtain 5-amidoisoxazoles with moderate yields. These heterocyclic compounds were tested in vitro MTT study to investigate inhibitive abilities to some cancer cell lines (C3a, L929, T98g and Mcf-7) and compounds 3a, 3c, 3e and 3h showed noticeable cytotoxic property against four cancer cell lines. (C) 2014 Elsevier Ltd. All rights reserved.</description>
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