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dc.contributor.authorKumari, C.-
dc.contributor.authorGoswami, A.-
dc.date.accessioned2022-06-23T13:46:40Z-
dc.date.available2022-06-23T13:46:40Z-
dc.date.issued2022-06-23-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/3545-
dc.description.abstractAn atom-economical approach for the synthesis of 3-aminofurans/thiophenes via a conjugate addition of alcohols and thiols with electron withdrawing groups (EWGs) at α positions on alkynenitriles followed by a modified Thorpe-Ziegler cyclization have been reported. This operationally simple protocol offers a rapid access to a library of 3-aminofurans/thiophenes in moderate to good yields.en_US
dc.language.isoen_USen_US
dc.subject3-Aminofuransen_US
dc.subject3-aminothiophenesen_US
dc.subjectAlkynenitrilesen_US
dc.subjectConjugate additionen_US
dc.subjectThorpe-Ziegler cyclizationen_US
dc.titleAccess to 5-Substituted 3-Aminofuran/Thiophene-2-Carboxylates from Bifunctional Alkynenitrilesen_US
dc.typeArticleen_US
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