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 |