<?xml version='1.0' encoding='utf-8'?>
<resource xmlns:xsi='http://www.w3.org/2001/XMLSchema-instance' xmlns='http://datacite.org/schema/kernel-3' xsi:schemaLocation='http://datacite.org/schema/kernel-3 http://schema.datacite.org/meta/kernel-3/metadata.xsd'>
<creators>
<creator>
<creatorName>Dinica, R.</creatorName>
</creator>
<creator>
<creatorName>Furdui, B.</creatorName>
</creator>
<creator>
<creatorName>Cârâc, G.</creatorName>
</creator>
<creator>
<creatorName>Stanciu, C.</creatorName>
</creator>
</creators>
<titles>
<title xml:lang='ro'>Fluorescent n-heterocycles via one-pot tandem reactions
</title>
</titles>
<publisher>Instrumentul Bibliometric National</publisher>
<publicationYear>2009</publicationYear>
<relatedIdentifier relatedIdentifierType='ISSN' relationType='IsPartOf'>1857-1727</relatedIdentifier>
<subjects>
<subject>microwave</subject>
<subject>“one-pot” reaction</subject>
<subject>indolizine</subject>
</subjects>
<dates>
<date dateType='Issued'>2009-10-05</date>
</dates>
<resourceType resourceTypeGeneral='Text'>Journal article</resourceType>
<descriptions>
<description xml:lang='en' descriptionType='Abstract'>Synthetic indolizines have attracted special attention in the past years mainly due to their manifold practical utilities. An improved preparation of bis-indolizines using microwave-assisted synthesis is described. The microwave-mediated three component reaction of acyl bromide, bipyridine and dipolarophyl is catalyzed by basic alumina to give corresponding bis-indolizines in excellent yields in a one –pot reaction.This strategy would provide access to fast synthesis of bis-indolizines which otherwise are accessible only through multistep synthesis. 
</description>
</descriptions>
<formats>
<format>application/pdf</format>
</formats>
</resource>