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Madavi S. Prasad on Muck Rack

Madavi S. Prasad

As seen in: Wiley Online Library, Royal Society of Chemistry
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Articles

Asymmetric Synthesis of spiro[benzofuran-pyrrolidine]-indolinedione via Bifunctional Urea Catalyzed [3+2]-annulation Reaction

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By L Raju Chowhan, Raghavaiah Pallepogu, Madavi S. Prasad, Biddika Anandarao
| Royal Society of Chemistry Verified
Asymmetric Synthesis of spiro[benzofuran-pyrrolidine]-indolinedione via Bifunctional Urea Catalyzed [3+2]-annulation Reaction In this study, we unveil a highly enantioselective [3+2] annulation protocol, adept at merging N-2,2,2-trifluoroethylisatin ketimines with 3-alkylidene benzofuranones under quinine-derived urea catalysis.
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Enantioselective Synthesis of Octahydrofuranoindole Core of Aspidosperma Alkaloids via a Diels‐Alder/Reduction/Fluoroetherification Reaction Sequence

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By Madavi S. Prasad, Murugesan Sivaprakash, L. Raju Chowhan, Sankar Bharani
| Wiley Online Library Verified
As a service to our authors and readers, this journal provides supporting information supplied by the authors. Such materials are peer reviewed and may be re-organized for online delivery, but are not copy-edited or typeset. Technical support issues arising from supporting information (other than missing files) should be addressed to the authors.
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N-2,2,2-trifluoroethylisatinketimine as a 1,2-dipolarophile for [3+2]- addition to access optically pure spirothiazolidine oxindoles

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By Prabha Vadivelu, L Raju Chowhan, Madavi S. Prasad, Sivaprakash Murugesan
| Royal Society of Chemistry Verified
N-2,2,2-trifluoroethylisatinketimine as a 1,2-dipolarophile for [3+2]- addition to access optically pure spirothiazolidine oxindoles Madavi S. Prasad, Sankar Bharani, Sivaprakash Murugesan, Prabha Vadivelu, Durairajan Siva Sundara Kumar and L Raju Chowhan Abstract The first report on using N-2,2,2-trifluoroethylisatinketimine as 1,2-dipolarophile for [3+2]-addition and the first asymmetric synthesis of N-2,2,2-trifluoroethylspirothiazolidine oxindoles is described.
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