Publication Type : Journal Article
Thematic Areas : Biotech
Publisher : Journal of Molecular Structure
Source : Journal of Molecular Structure, Volume 1127, p.498-510 (2017)
Url : https://www.sciencedirect.com/science/article/pii/S0022286016307918
Keywords : Chemical calculations, Formyl ketene dithioacetal, molecular dynamics, pyrimidine, Quantum, Single crystal XRD
Campus : Kochi
School : School of Pharmacy
Center : Biotechnology, Phytochemistry Labs
Department : Pharmaceutical Chemistry & Analysis
Year : 2017
Abstract : α-Formylketene dithioacetal is an active precursor for the synthesis of a variety of organic compounds including pyrimidines and its functionalized materials. The present study deals with the structural versatility of a solid representative compound from the family of α-formylketene dithioacetal to the formation of functionalized pyrimidines derivatives through experimental as well as theoretical methods. 2-(3,4-dimethoxybenzoyl)-3,3-bis(methylsulfanyl)prop-2-enal, the representative compound was synthesized with a reported protocol and characterized through spectral methods. The complete three dimensional solid state structural studies were carried out utilizing single crystal X-ray crystallographic technique along with theoretical methods like classical and accelerated molecular dynamics simulation. Various quantum chemical parameters were also discussed to reveals the complete molecular geometry and reactivity of designated compound.
Cite this Research Publication : M. Joy, Adeniyi, A. A., Mathews, A., Bijo Mathew, Prasanth, S., Soliman, M. E. S., Malayan, J. J., and Anabha, E. R., “Probing mechanism of α-formylketene dithioacetal towards the facile formation of functionalized pyrimidines: A structural approach”, Journal of Molecular Structure, vol. 1127, pp. 498-510, 2017.