Transition-Metal-Catalyzed C−C and C−Heteroatom Bonds Formation: Stereoselective Access to Functionalized Heterocycles

creativework.keywordsKeywordsen
dc.contributor.authorMaharana, Prabhat Kumar
dc.date.accessioned2026-02-18T12:03:40Z
dc.date.issued2025
dc.descriptionSupervisor: Punniyamurthy, Tharmalingam
dc.description.abstractThe thesis is divided into four chapters. The first chapter describes a general introduction on the synthesis of heterocycles utilizing transition-metal (TM) catalyzed ring opening cyclization of strained three-membered rings and cascade C-H functionalization/annulation strategy. The second chapter illustrates on a highly stereospecific synthesis of tetrahydro-[1,3,4]-oxadiazines via a Co-catalyzed C-N and C-O bonds formations of oxiranes with diaziridines. The third chapter focuses on a regiodivergent Cu-catalyzed cross-dimerization of oxaziridines with aziridines to synthesize functionally diverse [1,2,4]/[1,2,5]-oxadiazines. The fourth chapter deals with a Rh-catalyzed cascade C-H functionalization/annulation of benzamides with maleimides to furnish succinimide tethered isoquinoline-1,3-diones.
dc.identifier.otherROLL NO.196122020
dc.identifier.urihttps://gyan.iitg.ac.in/handle/123456789/3117
dc.language.isoen
dc.relation.ispartofseriesTH-3718
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/4.0/
dc.rights.urihttps://creativecommons.org/licenses/by-nc-sa/4.0/
dc.titleTransition-Metal-Catalyzed C−C and C−Heteroatom Bonds Formation: Stereoselective Access to Functionalized Heterocycles
dc.typeThesis

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