Biswajit Parhi

Employment

Employment history is unavailable.

Education

• Indian Institute of Science Education and Research Bhopal Doctor of Philosophy
  2013 - 2018

Projects & Funding

Projects & funding information is unavailable.

Publications (12)

• Preparation, characterization and dielectric properties of GO based ZnO embedded mixed metal oxides ternary nanostructured composites
  Journal of Alloys and Compounds 2021 DOI: 10.1016/j.jallcom.2021.159274
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• Surfactant free green synthesis of GOSiMa hybrid nanocomposite for charge storage application
  Ceramics International 2020 DOI: 10.1016/j.ceramint.2020.07.199
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• Application of quercetin flavonoid based hybrid nanocomposites: A review
  Saudi Pharmaceutical Journal 2020 DOI: 10.1016/j.jsps.2020.10.017
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• Cinchonamine Squaramide Catalyzed Asymmetric aza-Michael Reaction: Dihydroisoquinolines and Tetrahydropyridines
  Angewandte Chemie 2018 DOI: 10.1002/ange.201805020
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• Cinchonamine Squaramide Catalyzed Asymmetric aza-Michael Reaction: Dihydroisoquinolines and Tetrahydropyridines
  Angewandte Chemie International Edition 2018 DOI: 10.1002/anie.201805020
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• Catalytic Asymmetric Conjugate Addition of Carboxylic Acids via Oxa-Michael Reaction of Peroxy Hemiacetals followed by Kornblum DeLaMare Fragmentation
  Organic Letters 2016 DOI: 10.1021/acs.orglett.6b02463
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• ChemInform Abstract: Enantio- and Diastereoselective Synthesis of exo-Peroxyacetals: An Organocatalyzed Peroxyhemiacetalization/Oxa-Michael Addition Cascade.
  ChemInform 2016 DOI: 10.1002/chin.201645135
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• Correction to “Organocatalytic Enantioselective Intramolecular Oxa-Michael Reaction of Enols: Synthesis of Chiral Isochromene”
  The Journal of Organic Chemistry 2016 DOI: 10.1021/acs.joc.6b02177
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• ChemInform Abstract: Organocatalytic Enantioselective Intramolecular Oxa-Michael Reaction of Enols: Synthesis of Chiral Isochromenes.
  ChemInform 2016 DOI: 10.1002/chin.201634031
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• Organocatalytic Enantioselective Intramolecular Oxa-Michael Reaction of Enols: Synthesis of Chiral Isochromenes
  The Journal of Organic Chemistry 2016 DOI: 10.1021/acs.joc.6b00565
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