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A continuous-flow approach for the multi-gram scale synthesis of C2-alkyl- or β-amino functionalized 1,3-dicarbonyl derivatives and ondansetron drug using 1,3-dicarbonyls

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dc.contributor.author MOHANTA, NIRMALA en_US
dc.contributor.author NAIR, KRISHNA en_US
dc.contributor.author SUTAR, DASHARATH VISHAMBAR en_US
dc.contributor.author GNANAPRAKASAM, BOOPATHY en_US
dc.date.accessioned 2020-07-24T05:59:05Z
dc.date.available 2020-07-24T05:59:05Z
dc.date.issued 2020-08 en_US
dc.identifier.citation Reaction Chemistry & Engineering, 5(8), 1501-1508. en_US
dc.identifier.issn 2058-9883 en_US
dc.identifier.uri http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/4898
dc.identifier.uri https://doi.org/10.1039/D0RE00171F en_US
dc.description.abstract Continuous-flow chemistry is a modern technology that encompasses the green chemistry principles for the multi-gram synthesis of various API and drugs. Herein, we have developed a highly efficient and environmentally benign metal-free alkylation of 1,3-dicarbonyl compounds using secondary alcohols in the presence of inexpensive Amberlyst®-15 under continuous-flow. This method has a broad substrate scope with a variety of secondary alcohols and water as a byproduct. The Amberlyst®-15 is recyclable and reusable for the alkylation reaction under batch/continuous-flow technology. Furthermore, a continuous-flow technology driven Mannich reaction was demonstrated under an acid-free condition. In addition, a continuous-flow Fischer indole strategy for the ondansetron with an improved yield was demonstrated. Additionally, all these reactions were demonstrated with multi-gram scale synthesis without lowering the yield under batch/continuous-flow technology. en_US
dc.language.iso en en_US
dc.publisher Royal Society of Chemistry en_US
dc.subject Chemistry en_US
dc.subject TOC-JUL-2020 en_US
dc.subject 2020 en_US
dc.subject 2020-JUL-WEEK4 en_US
dc.title A continuous-flow approach for the multi-gram scale synthesis of C2-alkyl- or β-amino functionalized 1,3-dicarbonyl derivatives and ondansetron drug using 1,3-dicarbonyls en_US
dc.type Article en_US
dc.contributor.department Dept. of Chemistry en_US
dc.identifier.sourcetitle Reaction Chemistry & Engineering en_US
dc.publication.originofpublisher Foreign en_US


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