Madavi S. Prasad & M. Shiva Prasad

About

Our group research interests center around asymmetric synthesis of small natural products and mimics by exploiting catalysis. Our research also focuses to develop new synthetic methods to generate morphologically and functionally complex small chiral organic molecules with biological activity.

Employment

• University of Delhi Associate Professor of Organic Chemistry
  2025 - Present
• Central University of Tamil Nadu Assistant Professor
  2013 - 2025

Education

• Osmania University MSc
  2006 - 2008

Projects & Funding

Projects & funding information is unavailable.

Publications (21)

• Aminocatalytic, Stereoselective Synthesis of Tetrahydrocarbazole Spiropyrazolones via Remote [4 + 2] Annulation of Indole Tethered Enal With Olefinic Pyrazolones
  ChemistrySelect 2025 DOI: 10.1002/slct.202404935
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• Asymmetric synthesis of spiro[benzofuran-pyrrolidine]-indolinedione via bifunctional urea catalyzed [3 + 2]-annulation
  Organic & Biomolecular Chemistry 2025 DOI: 10.1039/D4OB01614A
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• Defluorinative Hydroxylation Promoted by Silica to Access Optically Pure Hexahydrofuranocarbazole via [4+2] Addition Reaction
  Asian Journal of Organic Chemistry 2025 DOI: 10.1002/ajoc.202400752
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• Amine Catalyzed Remote [4+2]‐annulation Of Indole Tethered Enal And Oxindole Olefin To Access Optically Pure Hydrocarbazole Spirooxindole Scaffolds
  Asian Journal of Organic Chemistry 2024 DOI: 10.1002/ajoc.202400061
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• Stereoselective Synthesis of Functionally Rich Spirooctahydroquinoline Oxindoles via Enynamide Cycloisomerisation/[4+2]‐Addition Sequence
  Advanced Synthesis & Catalysis 2024 DOI: 10.1002/adsc.202400162
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• Visible-light-induced organophotocatalytic and singlet oxygen-initiated domino construction of 1,4-dihydropyridines, C-3 functionalized spiro[indoline-3,4′-pyridines] and C-11 functionalized spiro[indeno-[1,2-b]quinoxaline-11,4′-pyridines]
  Organic & Biomolecular Chemistry 2023 DOI: 10.1039/D3OB00043E
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• Trienamine catalysed unprecedented remote olefin E/Z isomerisation/[4 + 2]-cycloaddition reaction to access spirooxindole hexahydroindoles
  Organic & Biomolecular Chemistry 2023 DOI: 10.1039/D2OB02228A
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• Stereoselective synthesis of CF3-containing spirocyclic-oxindoles using N-2,2,2-trifluoroethylisatin ketimines: an update
  RSC Advances 2023 DOI: 10.1039/D3RA00017F
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• N-2,2,2-Trifluoroethylisatin ketimine as a 1,2-dipolarophile for [3 + 2]-addition to access optically pure spirothiazolidine oxindoles
  Organic & Biomolecular Chemistry 2023 DOI: 10.1039/D3OB00685A
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• Asymmetric synthesis of the perhydroepoxyethanoindole core via sequential [4 + 2]-addition/reduction/fluoroannulation reactions
  Organic & Biomolecular Chemistry 2023 DOI: 10.1039/D2OB02058K
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