Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/15760
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dc.contributor.advisorSamanta, Sampak-
dc.contributor.authorLodhi, Rajni-
dc.date.accessioned2025-03-15T05:29:05Z-
dc.date.available2025-03-15T05:29:05Z-
dc.date.issued2025-02-25-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/15760-
dc.description.abstractThe main objective of this thesis work is to develop one-pot synthetic protocols for elegant access to pharmacologically attractive N-containing fused aza-heterocyclic scaffolds like cyclopropane-fused hydroindol-5-ones, indolizines, and α-carbolines involving simple and modifiable starting materials. The first chapter starts with the general introduction, which explains the synthesis and application of functionalized cyclopropane-fused hydroindol-5-one, indolizine, and α-carboline scaffolds with historical background and synthetic routes reported for the construction of an aforesaid class of aza-heterocyclic compounds via various synthetic modifications.en_US
dc.language.isoenen_US
dc.publisherDepartment of Chemistry, IIT Indoreen_US
dc.relation.ispartofseriesTH694;-
dc.subjectChemistryen_US
dc.titleDevelopment of POT-economy approaches to cyclopropane-fused-hydroindol-5-ones, indolizines and α-carbolinesen_US
dc.typeThesis_Ph.Den_US
Appears in Collections:Department of Chemistry_ETD

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