PS
Ponnusamy SHANMUGAM
CSIR-CLRI, CSIR-Central Leather Research Institute, Hokkaido University, Princeton University, National Institute for Interdisciplinary Science and Technology, University of Madras - Guindy Campus
0000-0003-0411-1982
Employment
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CSIR-CLRI Chief Scientist2020 - Present
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CSIR-Central Leather Research Institute Senior Principal Scientist2008 - 2020
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National Institute for Interdisciplinary Science and Technology Scientist1994 - 2008
Education
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Hokkaido University Post Doctoral- JSPS2002 - 2003
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Princeton University Post Doctoral1999 - 2000
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University of Madras - Guindy Campus Ph. D1989 - 1994
Projects & Funding
Projects & funding information is unavailable.
Publications (34)
- Bronsted and Lewis Acid-Catalyzed Diverse Functionalization of Indenoquinoxaline-11-Propargyl Alcohols: Synthesis of 4-Indeno-quinoxalinylidene-2,3-diarylcyclobutenone, 1,2-Dimethoxy-2-Aryl-ethylideneindenoquinoxaline, and 2-Methoxy-1-phenyldiaza-benzocy… Save
- Diverse Reactivity of 9‐Fluorene Propargylic Alcohol and 1,3‐Dicarbonyls with Bronsted and Lewis Acid Catalysts: Synthesis of Spiro, Conjugated, and 9‐Ethynyl Fluorene Derivatives Save
- Ferric chloride mediated synthesis, photophysical and in vitro anti-Alzheimer's properties of 1H-pyrrolo[2,3-b]pyridin-3-ylmethylphenyl-2-(9H-fluoren-9-ylidene)-1-phenylethan-1-imines Save
- Aza-Michael Addition of 2-Aminopyridine with 7-Aza-2-Indolone Chalconides: Synthesis of Functionalized α-Enaminones and One-Pot N-Alkenylation–Dearomatization of Pyridine Ring Save
- One‐Pot Functionalization at C‐2,2′‐Oxidation and C‐3,3′‐Bromination of 3,3′‐Bis‐7‐Azaindolylmethane Using NBS/CAN as a Reagent: Synthesis of Brominated 3,3′‐Bis‐7‐Aza‐2‐indalones Save
- Advances in 4-Hydroxycoumarin Chemistry: Functionalization, Prominent 4-Hydroxycoumarin-based Therapeutics and Their Pharmacological Significance Save
- Synthesis of Indenoquinoxalinone-5-(furano, pyrano, and oxepino)spiro Ethers from Alkenylated Propargyl Ethers of Indenoquinoxalinone via Ring-Closing Enyne Metathesis Save
- Synthesis of Dispiro‐[Indoline‐3,1′‐Cyclopropane‐2′,3′′‐Indoline]‐2,2′′‐Diones via Thermal [2+1] Cycloaddition Between 3‐Alkylidene‐7‐Aza‐2‐Indolones and 3‐Diazo‐7‐Aza‐2‐Oxindoles Save
- I2/p-TSA: An efficient reagent for regioselective synthesis of angularly fused diazabenzocyclo-pentafluorene via iodocyclisation of 11-(arylethynyl)-11H-indeno[1,2-b]quinoxalin-11-ol Save
- I2/CAN as a Mild and Efficient Reagent for Oxidative Csp3‐Csp2 Cleavage of 3,3′‐Bis‐7‐azaindolylmethane: A Rapid One‐Pot Access to 3‐Formyl and 3‐Iodo‐7‐azaindoles Save