Noble V Thomas

Assistant Professor
Email: noble@cmscollege.ac.in

Education

  • BSc, MG University, 2012
  • MSc, MG University 2015
  • PhD – (Thesis Submitted), University of Kerala, 2022
  • 1,3-Dipolar cycloaddition reactions
  • Synthesis of small organic molecules
  • Design and synthesis of fuctionalized organic compounds
  • AN1924303 Green Chemistry
  • CH1924301 Chemistry of Materials and metal organic frameworks
  • CH1924302 Green Alternatives to Organic synthesis and Stereoselective transformations
  • AC1924303Green Chemistry and Nanotechnology

Publications

  1. Thomas, N. V., Meenakshy, C. B., Leena, S., & Deepthi, A. Stereoselective synthesis of dispirooxindoles incorporating Pyrrolo [2, 1-a] isoquinoline via [3+ 2] cycloaddition of azomethine ylides with a thiazolo [3, 2-a] indole dipolarophile. Synthesis (Thieme),2022, 54(12), 2885-2893.

https://www.thieme-connect.com/products/ejournals/abstract/10.1055/a-1777-2423

  1. Thomas, N. V., Sathi, V., & Deepthi, A. Stereoselective synthesis of dispiroindano pyrrolidines by the [3+2] cycloaddition of thiazolo [3, 2‐a] indole tethered dipolarophile with azomethine ylides. Journal of Heterocyclic Chemistry (Wiley), 2022, https://onlinelibrary.wiley.com/doi/10.1002/jhet.4481
  2. Thomas, N. V., Vidya S, Deepthi, A., Sudheendran Leena, S., & Chopra, S. Engaging thieno [2, 3‐b] indole‐2, 3‐dione for the efficient synthesis of spiro [indoline‐3, 4′‐thiopyrano [2, 3‐b] indole] by reaction with N‐substituted isatilidenes, Journal of Heterocyclic Chemistry (Wiley), 2021, 58(1), 48-55.
  3. Deepthi, A., Thomas, N. V., & Sruthi, S. L. An overview of the reactions involving azomethine imines over half a decade, New Journal of Chemistry (RSC), 2021, 45(20), 8847-8873.
  4. Vidya S, Thomas, N. V., & Deepthi, A. Stereoselective synthesis of dispiro heterocycles by [3+ 2] cycloaddition of azomethine ylides with a thiazolo [3, 2-a] indole derivative, Organic & Biomolecular Chemistry (RSC), 2020, 18(39), 7822-7826.
  5. Deepthi, A., Thomas, N. V., &Vidya S. Green Protocols for the synthesis of 3, 3’- spirooxindoles–2016-mid 2019, Current Green Chemistry (Bentham), 2019, 6(3), 210-225.
  6. Vidya S, Deepthi, A. &Thomas, N. V. An unprecedented synthesis of 3, 3‐disubstituted isochroman‐1, 4‐diones using nitrones as oxygen atom donors, Journal of Heterocyclic Chemistry (Wiley), 2019, 56(9), 2333-2340.

Contributions to the Academic Conferences (Poster/Oral Presentations)

  1. Noble V Thomas and Ani Deepthi, “Synthesis of dispiroheterocycles using azomethine ylide derived from tetrahydro isoquinolines in methanol” in the International Webinar on Recent Advances in Experimental and Computational Bioorganic Chemistry- RABoC 2021, Department of Chemistry, University of Kerala, March 18 – 20th, 2021.
  2. Noble V Thomas and Ani Deepthi, “Cycloaddition reactions of thiazolo[3,2-a]indole derivatives with various azomethine ylides to yield pyrrolo[2,1-a]isoquinolines” at International Conference on Materials for the Millennium – MATCON 2021, Cochin University (CUSAT) during March 15 – 19th, 2021.
  3. Noble V Thomas and Ani Deepthi, “Synthesis of dispiropyrrolizidines from thiazolo[3,2-a]indole derivative via cycloaddition with various azomethine ylides” in the International Webinar- Neoteric Advances in Chemical Sciences -NACS 2020, Department of Chemistry, University of Kerala, December 17 – 19th2020.
  4. Noble V Thomas and Ani Deepthi, “Synthesis of Spirooxindole Incorporated Thiopyrans from Thieno[2,3-b] indole-2,3-dione” at National Seminar on Current Trends in Chemistry (CTriC 2020), t Cochin University CUSAT February 6 – 7th2020.
  5. Noble V Thomas and Ani Deepthi, “A Novel Reactivity Of Thieno[2,3 –b]Indole-2,3-Dione” in the International Conference on Materials for the Millennium – MATCON 2019, Cochin University CUSAT, March 14 -16th, 2019.
  6. Noble V Thomas and Ani Deepthi, “NHC CATALYSED REACTIONS OF TRICARBONYL COMPOUNDS” in the National seminar on Neoteric Advances in Chemical Sciences -NACS 2018, Department of Chemistry, University of Kerala, October 11 – 12th, 2018.

Chemistry
Department