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सीएसआईआर - उत्तर पूर्व विज्ञान एवं प्रौद्योगिकी संस्थान
CSIR-North East Institute of Science and Technology

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Particulars of organization, functions and duties

Dr. Atul Ashok More

Dr. Atul Ashok More

Designation : Scientist D

Education : Ph.D. (Prof. Ramana’s LaboratoryCSIR-NCL, Pune, India), Postdoc (Prof. Alex Szpilman’s LaboratoryAriel University, Israel)

ID. No.: 1307

Email id : atulmore@neist.res.in, atulmore1@gmail.com


Research Interest

Electrochemical synthesis, Catalysis, Total synthesis of biologically active complex natural products. Process development for drug molecules and chemical biology

Projects

  • Cascade Enantioselective Ring Opening of Saturated Heterocycles: An Easy Access to Indomethacin, Euroticins, Agesamides, and their Analogs for Anti-Inflammatory and Cytotoxic Activity". (GPP0409)
  • Development of Cost-Effective and Green Methods for the Preparation of Hepatitis Medicines: CSIR-RDSF Seed fund Grant (IHP 0007)
  • Thin –flim nanocomposite membrance technology for CO2 separation
  • Innovative Processes and Technologies for Crop Protection Chemicals (Agromission-2)
  • Natural products/ herbal formulations/ APIs/ agrochemicals and their allied for value addition

List of Publications

  • Baruah, Ashitosh; Baruah, Mainee; Bulbul, Rassel M.; Dey, Sandeep Kumar; More, Atul Lewis Acid Catalyzed Switchable Functionalization of C,N-Cyclic Ketimines with Vinyl Azides: Access to Diverse C(2) Alkylated Pseudoindoxyls
  • Swagota Paul, Ashitosh Baruah, and Atul A. More* Divergent Reactivity of Iminyl Radicals in Four Interrupted Pathways for the Synthesis of Cyclic/Acyclic Ketones and N‑Heterocycles from Vinyl Azides and Phenylacetic Acids Journal of Organic Chemistry 89 13128−13136 2024
  • Atul A. More and Alex M. Szpilman* Indium(III) Catalyzed Reactions of Vinyl Azides and Indoles. Organic Letters 22 3759-3764 2020
  • Atul A. More, Sourav K. Santra, and Alex M. Szpilman* Azido-Enolonium Species in C−C and C−N Bond-Forming Coupling Reactions. Organic Letters 22 768-771 2020
  • Atul A More, G. Pathe, K. Parida, S. Maksymenko, Y. B. Lipisa, and Alex M. Szpilman* α-N-Heteroarylation and α Azidation of Ketones via Enolonium Species. Journal of Organic Chemistry 83 2442–2447 2018
  • S. Arava, S. Maksymenko K. Parida G. Pathe Atul A More, Y. B Lipisa, and Alex M Szpilman* A Two-Step Protocol for Umpolung Functionalization of Ketones Via Enolonium Species Journal of Visualized Experiments 138 e57916 2018
  • S. Maksymenko K. Parida G. Pathe Atul A More, Y. B Lipisa, and Alex M Szpilman* Transition-Metal-Free Intermolecular α-Arylation of Ketones via Enolonium Species. Organic Letters 19 6312–6315 2017
  • Atul A More and Chepuri V Ramana* Alkyne [2+2+2]-Cyclotrimerization Approach for Synthesis of 6,7 Cyclopropylallocolchicinoids. Journal of Organic Chemistry 81 3400–3406 2016
  • Atul A More and Chepuri V Ramana* Total Synthesis of Integrastatin B Enabled by a Benzofuran Oxidative Dearomatization Cascade. Organic Letters 18 1458–1461 2016
  • Atul A More and Chepuri V Ramana* o Quinone Methides via Oxone-Mediated Benzofuran Oxidative Dearomatization and Their Intramolecular Cycloaddition with Carbonyl Groups: An Expeditious Construction of the Central Tetracyclic Core of Integrastatins, Epicoccolide A, and Epicocconigrone A. Organic Letters 18 612–615 2016
  • Atul A More and Chepuri V Ramana* Total Synthesis of the Putative Structure of Xylarinol B. Chemistry-an Asian Journal 9 1557-1562 2014

List of Key Patents with brief description

  • A novel process for the preparation of N (heterocyclic) cyclopropanecarboxamide derivatives via oxidative ring-editing transformation of cyclobutanone derivatives.
  • Bridged bicyclic compounds, process for preparation and use thereof Atul A More and Chepuri V Ramana* 2017, IN 2015DE02685 A 20170303 03rd March 2017 Indian Pat. Appl. Approved
  • A novel process for the preparation of benzofuran derivatives Atul A More and Chepuri V Ramana* 2017, IN 2015DE02333 A 2017020303rd March 2017 Indian Pat. Appl. Approved

Personal Website

https://sites.google.com/view/more-research-group/home