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DC Field | Value | Language |
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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 |
Appears in Collections: | JOURNAL ARTICLES |
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