DSpace logo

Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/15553
Full metadata record
DC FieldValueLanguage
dc.contributor.authorKumar, Indresh-
dc.date.accessioned2024-09-12T09:36:27Z-
dc.date.available2024-09-12T09:36:27Z-
dc.date.issued2021-
dc.identifier.urihttps://pubs.rsc.org/en/content/articlehtml/2021/cc/d0cc06357f-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/15553-
dc.description.abstractThe synthesis of β-(C3)-functionalized pyrroles is a challenging task and requires a multistep protocol. An operationally simple direct catalytic synthesis of β-substituted pyrroles has been developed. This one-pot multicomponent method combined aqueous succinaldehyde as 1,4-dicarbonyl, primary amines, and isatins to access hydroxyl-oxindole β-tethered pyrroles. Direct synthesis of the β-substituted free NH-pyrrole is the central intensity of this work. DFT-calculations and preliminary mechanism investigation support the possible reaction pathway.en_US
dc.language.isoenen_US
dc.publisherRSCen_US
dc.subjectChemistryen_US
dc.subjectSynthesisen_US
dc.subjectPaal–Knorr reactionen_US
dc.titleDirect catalytic synthesis of β-(C3)-substituted pyrroles: a complementary addition to the Paal–Knorr reactionen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.