<efrbr:recordSet xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:efrbr="http://vfrbr.info/efrbr/1.1" xmlns:efrbr-work="http://vfrbr.info/efrbr/1.1/work" xmlns:efrbr-expression="http://vfrbr.info/efrbr/1.1/expression" xmlns:efrbr-manifestation="http://vfrbr.info/efrbr/1.1/manifestation" xmlns:efrbr-person="http://vfrbr.info/efrbr/1.1/person" xmlns:efrbr-corporateBody="http://vfrbr.info/efrbr/1.1/corporateBody" xmlns:efrbr-concept="http://vfrbr.info/efrbr/1.1/concept" xmlns:efrbr-structure="http://vfrbr.info/efrbr/1.1/structure" xmlns:efrbr-responsible="http://vfrbr.info/efrbr/1.1/responsible" xmlns:efrbr-subject="http://vfrbr.info/efrbr/1.1/subject" xmlns:efrbr-other="http://vfrbr.info/efrbr/1.1/other" xsi:schemaLocation="http://vfrbr.info/efrbr/1.1 http://vfrbr.info/schemas/1.1/efrbr.xsd"><efrbr:entities><efrbr-work:work identifier="http://purl.tuc.gr/dl/dias/B90E479C-48D7-4FC2-A16E-91B416B5ED71"><efrbr-work:titleOfTheWork> Synthesis of quinoxalines by cyclization of α-arylimino oximes of α-dicarbonyl compounds</efrbr-work:titleOfTheWork></efrbr-work:work><efrbr-expression:expression identifier="http://purl.tuc.gr/dl/dias/B90E479C-48D7-4FC2-A16E-91B416B5ED71"><efrbr-expression:titleOfTheExpression> Synthesis of quinoxalines by cyclization of α-arylimino oximes of α-dicarbonyl compounds</efrbr-expression:titleOfTheExpression><efrbr-expression:formOfExpression vocabulary="DIAS:TYPES">
            Peer-Reviewed Journal Publication
            Δημοσίευση σε Περιοδικό με Κριτές
         </efrbr-expression:formOfExpression><efrbr-expression:dateOfExpression type="issued">2015-10-21</efrbr-expression:dateOfExpression><efrbr-expression:dateOfExpression type="published">2000</efrbr-expression:dateOfExpression><efrbr-expression:languageOfExpression vocabulary="iso639-1">en</efrbr-expression:languageOfExpression><efrbr-expression:summarizationOfContent>Heating the title compounds 1 at reflux in acetic anhydride yields quinoxalines 3 and 4 via a presumed aryliminoiminyl radical 5, resulting from homolytic cleavage of the NO bond in the intermediate ester 2. The observed regioselectivity of the reaction is also rationalized by implicating such a radical.</efrbr-expression:summarizationOfContent><efrbr-expression:useRestrictionsOnTheExpression type="creative-commons">http://creativecommons.org/licenses/by/4.0/</efrbr-expression:useRestrictionsOnTheExpression><efrbr-expression:note type="journal name">Tetrahedron Letters</efrbr-expression:note><efrbr-expression:note type="journal volume">41</efrbr-expression:note><efrbr-expression:note type="journal number">52</efrbr-expression:note><efrbr-expression:note type="page range">10299-10302</efrbr-expression:note></efrbr-expression:expression><efrbr-person:person identifier="http://users.isc.tuc.gr/~nxekoukoulotakis"><efrbr-person:nameOfPerson vocabulary="TUC:LDAP">
            Xekoukoulotakis Nikos
            Ξεκουκουλωτακης Νικος
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            A.J Maroulis
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             C.P Hadjiantoniou-Maroulis
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            Elsevier
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