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               <dc:title>Eco-Friendly Methodology to Prepare N-Heterocycles Related to Dihydropyridines: Microwave-Assisted Synthesis of Alkyl 4-Arylsubstituted-6-chloro-5-formyl-2-methyl-1,4-dihydropyridine-3-carboxylate and 4-Arylsubstituted-4,7-dihydrofuro[3,4-b]pyridine-2,5(1H,3H)-dione</dc:title>
               <dc:creator>Rodríguez Cabrera, Hortensia María</dc:creator>
               <dc:creator>Martin, Osnieski</dc:creator>
               <dc:creator>Suárez, Margarita</dc:creator>
               <dc:creator>Martín, Nazario</dc:creator>
               <dc:creator>Albericio Palomera, Fernando</dc:creator>
               <dc:subject>Escalfament per microones</dc:subject>
               <dc:subject>Molècules</dc:subject>
               <dc:subject>Química verda</dc:subject>
               <dc:subject>Calefacció</dc:subject>
               <dc:subject>Microwave heating</dc:subject>
               <dc:subject>Molecules</dc:subject>
               <dc:subject>Green chemistry</dc:subject>
               <dc:subject>Heating</dc:subject>
               <dc:description>Here we describe the efficient synthesis of alkyl 4-arylsubstituted-6-chloro-5-formyl-2-methyl-1,4-dihydropyridine-3-carboxylates and 4-arylsubstituted-4,7-dihydro-furo[3,4-b]pyridine-2,5(1H,3H)-diones via microwave-accelerated reaction of alkyl 4-arylsubstituted-2-methyl-6-oxo-1,4,5,6-tetrahydro-3-pyridinecarboxylates with the appropriate reagents. This eco-friendly approach to these valuable dihydropyridine derivatives does not involve the harsh or highly contaminating conditions common in classical heating and offers a reduction or even elimination of solvent use and recovery, simplification of the work-up procedures, facility of scale up, and low energy consumption, in addition to moderate to higher yields.</dc:description>
               <dc:date>2020-03-11T17:16:37Z</dc:date>
               <dc:date>2020-03-11T17:16:37Z</dc:date>
               <dc:date>2011-11-21</dc:date>
               <dc:date>2020-03-11T17:16:37Z</dc:date>
               <dc:type>info:eu-repo/semantics/article</dc:type>
               <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
               <dc:relation>Reproducció del document publicat a: https://doi.org/10.3390/molecules16119620</dc:relation>
               <dc:relation>Molecules, 2011, vol. 16, num. 11, p. 9620-9635</dc:relation>
               <dc:relation>https://doi.org/10.3390/molecules16119620</dc:relation>
               <dc:rights>cc-by (c) Rodríguez, Hortensia et al., 2011</dc:rights>
               <dc:rights>http://creativecommons.org/licenses/by/3.0/es</dc:rights>
               <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
               <dc:publisher>MDPI</dc:publisher>
               <dc:source>Articles publicats en revistes (Química Inorgànica i Orgànica)</dc:source>
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